Sterility Testing Consumables, Media & Instruments
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Casein peptone Lecithin Polysorbate Broth
NACRES: NA.85
Кат. номер 22089-500G-F 22089-VAR-F 22089-100G-F ApplicationFor the dilution of samples from pharmaceutical, cosmetic and raw material or end-products, for the purpose of enumeration.Preparation NoteSuspend 25 g in 960 ml distilled water. Heat in a water-bath at 50°C for approx. 30 minutes until completely dissolved. Add 40 ml polysorbate (TWEEN® 20) and sterilize by autoclaving at 121°C for 15 minutes.Other NotesMicrobial limit testsFootnoteWe offer two media types: the superior granulated GranuCult® and the cost-efficient powdered NutriSelect® culture media, depending on your needs.
The designations basic, plus, or prime are added to indicate the quality control level, from basic quality control to standard QC plus to prime for full regulatory compliance.Legal InformationGRANUCULT is a registered trademark of Merck KGaA, Darmstadt, Germany
NutriSelect is a registered trademark of Merck KGaA, Darmstadt, Germany
TWEEN is a registered trademark of Croda International PLCПараметрыQuality Level 200 sterility non-sterile form powder shelf life limited shelf life, expiry date on the label composition casein peptone, 20.0 g/L , soya lecithin, 5.0 g/L Торговая марка NutriSelect® Plus application(s) microbiological culture: suitable, microbiology: suitable, sterility testing: suitable, surface monitoring: suitable final pH 7.1±0.5 (25 °C) Featured Industry Cleaning Products
Cosmetics
Environmental
Food and Beverages
Personal Care
Pharmaceuticalsuitability nonselective for Bacillus spp., nonselective for Candida spp., nonselective for Clostridium spp., nonselective for Escherichia coli, nonselective for Staphylococcus spp., nonselective for Streptococcus spp., nonselective for bacteria (General Media), nonselective for coliforms, nonselective for molds (General Media), nonselective for yeasts (General Media)
Safety InformationPersonal Protective Equipment Eyeshields, Gloves, type N95 (US) RIDADR NONH for all modes of transport WGK Germany WGK 1 Flash Point F Not applicable Flash Point C Not applicable Узнать цену -
Clear Fluid Thioglycollate Medium STBMCTM12
eCl@ss: 32014001 NACRES: NA.74 General descriptionClear Thioglycollate medium has the same growth promotion properties as the standard Fluid Thioglycollate Medium (FTM). The alternative formulation brings extra visual clarity versus the FTM which has a slight turbidity or haze. Composition and growth performance of this medium comply with the European Pharmacopeia (EP) 2.6.1, United States Pharmacopeia (USP) 71 and Japanese Pharmacopeia (JP) 4.06. Our manufacturing approach ensures the highest level of quality for our media, improving accuracy and significantly reducing the risk of incorrect interpretation and false results. The appearance of the fluid is light yellow and viscous liquid with a pink ring in suspension ≤1 cm. The pH of the product is 7.1 ± 0.2 and can be stored at 2-25°C for 12 months. The incubation temperature varies between 30-35°C, with an incubation time of 7-14 days. One box of product contains 12 bottles of 100mL of Medium. Each bottle has a screw cap with a septum that minimizes the risks of cross-contamination and optimizes the disinfection procedures.ApplicationClear Fluid Thioglycollate Medium is intended for the detection of anaerobic bacteria however, it also enables aerobic bacterial detection. This medium is used for sterility testing by membrane filtration or direct inoculation. The QC organisms include Clostridium sporogenes (ATCC 19404), Staphylococcus aureus (ATCC 6538) and Pseudomonas aeruginosa (ATCC 9027).
Sterility testing (membrane filtration and direct inoculation)
Bioburden testingComponentsScrew cap with septumSpecificationsIncubation Time: 7–14 daysLegal InformationSTERITEST is a registered trademark of Merck KGaA, Darmstadt, GermanyПараметрыstorage conditions Room Temperature (2 to 25 °C) Quality Level 400 Agency/Method in accordance with EP 2.6.1, in accordance with JP 4.06, in accordance with USP 71 sterility sterile; autoclaved form liquid shelf life 12 mo. feature ready-to-use packaging pkg of 100 mL (12 Bottles with screw cap and septum) application(s) sterility testing: suitable volume size 100 mL input sample type pharmaceutical(s) pH 7.1±0.2 (25.0 °C) test parameters sample volume: 100 mL Featured Industry Cosmetics
Food and Beverages
Pharmaceuticalcompatibility for use with Steritest® shipped in ambient storage temp. 2-25°C suitability aerobic bacteria, nonselective for
Safety InformationWGK Germany WGK 1 Flash Point F Not applicable Flash Point C Not applicable 159,78 € / 15 592 ₽Получить предложение -
Dey-Engley neutralizing broth
NACRES: NA.85
Кат. номер D3435-500G D3435-VAR ApplicationDey-Engley neutralizing broth has been used to premoisten the sponge swab samples to neutralise the residual action of the disinfectants on the microbiological growth. It has also been used to resuspend the Vermamoeba (Hartmannella) vermiformis cysts to neutralize peracetic acid (PAA).
Dey-Engley Neutralizing Broth is used in disinfectant testing where neutralization of the antiseptics and disinfectants is important for determining bactericidal activity.Biochem/physiol ActionsThe Dey-Engley Neutralizing Broth neutralizes a broad spectrum of antiseptics and disinfectants including, quaternary ammonium compounds, phenolics, iodine, chlorine, mercurials, formaldehyde and glutaraldehyde. Sodium thioglycollate, sodium thiosulphate, sodium bisulphite, soya lecithin and polysorbate 80 act as neutralizing components. Growth is indicated by a color change from purple to yellow.ComponentsIngredients(g/L)
Casein enzymatic hydrolysate5.00
Yeast extract2.50
Dextrose10.00
Sodium thiosulfate6.00
Sodium thioglycollate1.00
Sodium bisulfite2.50
Lecithin7.00
Polysorbate 805.00
Bromocresol purple0.02Preparation NoteSuspend 39 g of Dey-Engley Neutralizing Broth in 1000 ml of distilled water. Boil to dissolve the medium completely. Sterilize by autoclaving 15 lbs. pressure (121°C) for 15 minutes.FootnoteWe offer two media types: the superior granulated GranuCult® and the cost-efficient powdered NutriSelect® culture media, depending on your needs.
The designations basic, plus, or prime are added to indicate the quality control level, from basic quality control to standard QC plus to prime for full regulatory compliance.Legal InformationGRANUCULT is a registered trademark of Merck KGaA, Darmstadt, Germany
NutriSelect is a registered trademark of Merck KGaA, Darmstadt, GermanyПараметрыQuality Level 200, 100 sterility non-sterile form powder shelf life limited shelf life, expiry date on the label Торговая марка NutriSelect® Plus application(s) microbiological culture: suitable, microbiology: suitable, sterility testing: suitable, surface monitoring: suitable final pH 7.6±0.2 (25 °C) Featured Industry Environmental
Food and Beverages
Pharmaceuticalstorage temp. 2-8°C suitability nonselective for Bacillus spp., nonselective for Escherichia coli, nonselective for Pseudomonas spp., nonselective for Salmonella spp., nonselective for Staphylococcus spp., nonselective for bacteria (General Media), nonselective for coliforms
Safety Informationpictograms GHS07 signalword Warning hcodes H317 pcodes P261 - P272 - P280 - P302 + P352 - P333 + P313 - P362 + P364 Personal Protective Equipment Eyeshields, Faceshields, Gloves RIDADR NONH for all modes of transport WGK Germany WGK 3 Flash Point F Not applicable Flash Point C Not applicable Узнать цену -
Diamond cutting file kit SYMBDFS01
General descriptionThe Diamond cutting file kit is an optional accessory of Steritest® ampoule breaker.ApplicationDiamond cutting file kit is used with glass ampoules.Legal InformationSTERITEST is a registered trademark of Merck KGaA, Darmstadt, GermanyПараметрыmaterial 316L stainless steel , polyphenylsulfone (PPSU) (Screw) Agency/Method EP (2.6.1), JP (4.06), USP (71) Торговая марка Steritest® application(s) sterility testing: suitable input pharmaceutical(s) Featured Industry Pharmaceutical compatibility for use with Steritest® Symbio pump shipped in ambient Узнать цену -
Fluid A, Double packed STBMRFA12DP
eCl@ss: 32014001 NACRES: NA.74 General descriptionFluid A is a general rinse buffer in compliance with the European Pharmacopeia (EP) 2.6.1, United States Pharmacopeia (USP) 71 and Japanese Pharmacopeia (JP) 4.06. The sterilized double Tyvek® packaging increases the test method reliability, allowing to streamline the cleaning procedures, minimize the risk of cross-contamination in laminar flow hoods and secure an efficient decontamination of isolator chambers. The product is a clear colorless liquid with a pH of 7.1 ± 0.2 at 25°C. It can be stored at 2-25°C (protected from light) for 12 months. A single box contains 12 bottles of 100ml of fluid, each bottle with a screw cap with septum closure that reduces the risk of cross-contamination and optimizes the disinfection procedures.ApplicationSterility testing
Bioburden testing
Fluid A is used to rinse aqueous solutions during sterility testing by membrane filtration. It is also used to dilute soluble solids for the same application. This product is recommended as a rinsing fluid for membrane filtration of non-sterile products. It is excellent for dissolving or diluting samples, reconstituting commercial microorganisms, or as a transport medium for microorganisms.ComponentsScrew cap with septumCulture MediumFluid ALegal InformationSTERITEST is a registered trademark of Merck KGaA, Darmstadt, Germany
Tyvek is a registered trademark of E. I. du Pont de Nemours and CompanyПараметрыstorage conditions Room Temperature (2 to 25 °C) Quality Level 400, Agency/Method in accordance with EP 2.6.1, in accordance with JP 4.06, in accordance with USP 71 sterility sterile; ethylene oxide treated form liquid feature ready-to-use packaging pkg of 100 mL (Bottle with screw cap and septum), pack of 12 bottles application(s) sterility testing: suitable volume size 100 mL color clear, with no precipitate and free of visible particles input sample type pharmaceutical(s) pH 7.1±0.2 (25.0 °C) Featured Industry Pharmaceutical compatibility for use with Steritest® shipped in ambient storage temp. 2-30°C suitability nonselective for
Safety InformationWGK Germany WGK 1 Flash Point F Not applicable Flash Point C Not applicable 120,75 € / 11 783 ₽Получить предложение -
Fluid K STBMRFK34
eCl@ss: 32014001 NACRES: NA.74 General descriptionFluid K is suitable for testing specimens that contain petrolatum, oils, or oily solutions. The fluids composition complies with the European Pharmacopeia (EP) 2.6.1, United States Pharmacopeia (USP) 71 and Japanese Pharmacopeia (JP) 4.06. This is a light-yellow liquid with a pH of 6.9 ± 0.2 at 25°C. It can be stored at 15-25°C (protected from light) for 12 months. A single box contains 4 bottles of 300 mL of fluid, each bottle with a screw cap with septum closure that reduces the risk of cross-contamination and optimizes the disinfection procedures.ApplicationSterility testing
Bioburden testing
Fluid K is used as diluting or rinsing fluid for sterility testing on samples containing petrolatum/oil. It can be used in combination with the STERITEST® sterility testing system and in bioburden testing to rinse membranes and dilute/dissolve samples. The fluid can also be excellent for rinsing pathways of medical devices, and for samples that are difficult to filter or dissolve.ComponentsScrew cap with septumCulture MediumFluid KLegal InformationSTERITEST is a registered trademark of Merck KGaA, Darmstadt, GermanyПараметрыstorage conditions Room Temperature (2 to 25 °C) Quality Level 400 Agency/Method in accordance with EP 2.6.1, in accordance with JP 4.06, in accordance with USP 71 sterility sterile; autoclaved form liquid shelf life 12 mo. feature ready-to-use packaging pkg of 300 mL (Bottle with screw cap and septum), pack of 4 bottles application(s) sterility testing: suitable volume size 300 mL color light, with no precipitate and free of visible particles input sample type pharmaceutical(s) pH 6.9±0.2 (25.0 °C) Featured Industry Pharmaceutical compatibility for use with Steritest® shipped in ambient storage temp. 2-30°C suitability nonselective for
Safety InformationWGK Germany WGK 2 Flash Point F Not applicable Flash Point C Not applicable 172,73 € / 16 855 ₽Получить предложение -
Fluid Thioglycollate Medium STBMFTM12
eCl@ss: 32014001 NACRES: NA.74 General descriptionFluid Thioglycollate Medium (FTM) is a critical component of our STERITEST® solution. Composition and growth performance of this medium comply with the European Pharmacopeia (EP) 2.6.1, United States Pharmacopeia (USP) 71 and Japanese Pharmacopeia (JP) 4.06. Our manufacturing approach ensures the highest level of quality for our media, improving accuracy and significantly reducing the risk of incorrect interpretation and false results. The appearance of the fluid is light-yellow, slightly opalescent and viscous liquid with a pink ring in suspension 1 cm. The pH of the product is 7.1 ± 0.2 and can be stored at 2-25°C. The incubation temperature varies between 30-35°C, with an incubation time of 7-14 days. The product is supplied as 12 bottles of 100 mL of medium, screw cap with septum closure that minimizes the risks of cross-contamination and optimizes the disinfection procedures.ApplicationFluid Thioglycollate Medium (FTM) is primarily used for the detection of anaerobic bacteria. However, it also enables aerobic bacterial detection. The QC organisms include Clostridium sporogenes (ATCC 19404; ATCC 11437), Staphylococcus aureus (ATCC 6538) and Pseudomonas aeruginosa (ATCC 9027). This medium is used for sterility testing by membrane filtration or direct inoculation.
Sterility testing (membrane filtration and direct inoculation)
Bioburden testingComponentsScrew cap with septumCulture MediumFluid ThioglycollateAnalysis NoteTurbidity indicates growthLegal InformationSTERITEST is a registered trademark of Merck KGaA, Darmstadt, GermanyПараметрыstorage conditions Room Temperature (2 to 25 °C) Quality Level 400 Agency/Method in accordance with EP 2.6.1, in accordance with JP 4.06, in accordance with USP 71 sterility sterile; autoclaved form liquid shelf life 12 mo. feature ready-to-use packaging pkg of 100 mL, pack of 12 bottles application(s) sterility testing: suitable volume size 100 mL input sample type pharmaceutical(s) pH 7.1±0.2 (25 °C) Featured Industry Pharmaceutical compatibility for use with Steritest® shipped in ambient storage temp. 2-30°C suitability anaerobic bacteria, nonselective for
Safety InformationWGK Germany WGK 1 Flash Point F Not applicable Flash Point C Not applicable 159,78 € / 15 592 ₽Получить предложение -
Milliflex® PLUS Pump MXPPLUVHP
NACRES: NB.79 General descriptionThe compact Milliflex® PLUS VHP vacuum pump streamlines filtration steps during testing to accelerate and ease the sample preparation. When used with convenient Milliflex® filtration funnels, the pump and Milliflex® units comprise an integrated solution for delivering reliable and accurate results. The pumps small footprint suits tight workspaces and its low profile allow easy access and usage in isolators. The housing and the external parts are VHP resistant.ApplicationThe VHP Resistant Milliflex® PLUS Pump is designed to perform filtrations of samples inside an isolator. It is suitable for rapid sterility testing in combination with the Milliflex® Rapid System.Features and Benefits- Streamlines filtration steps
- Can be used with the Milliflex® filtration funnels
- Compatible with the isolator environment and VHP decontamination
- Compatible with the Milliflex® Rapid System to perform rapid sterility testing in a clean environment (isolator)
Legal InformationMILLIFLEX is a registered trademark of Merck KGaA, Darmstadt, GermanyПараметрыТорговая марка Milliflex® application(s) bioburden testing: suitable, sterility testing: suitable, water monitoring: suitable input sample type pharmaceutical(s) Featured Industry Pharmaceutical compatibility for use with Milliflex® Systems, standard for VHP shipped in ambient Узнать цену -
Silicone drain tubing SYMBTBG01
eCl@ss: 32014001 NACRES: NB.24 General descriptionThe silicone drain tube is an accessory for STERITEST® Symbio pumps. One end of the drain tubing is connected to the drain tray of the pump and the other end is directly placed into the waste container or isolator table drain (depending on the pump version). It is autoclavable (121°C for 30 minutes or 134°C for 10 minutes).ApplicationThe silicon drain tubing is an accessory for STERITEST® Symbio pumps and is used for liquid disposal.Legal InformationSTERITEST is a registered trademark of Merck KGaA, Darmstadt, GermanyПараметрыmaterial silicone Agency/Method EP 2.6.1, JP 4.06, USP 71 Торговая марка Steritest® application(s) sample preparation: suitable, sterility testing: suitable input sample type pharmaceutical(s) Featured Industry Pharmaceutical compatibility for use with Steritest® Compact Pump, for use with Steritest® Equinox Isofit Pump, for use with Steritest® Equinox Pump, for use with Steritest® Integral Pump, standard for VHP shipped in ambient Узнать цену -
Steridilutor® NEO Device TZA000010
eCl@ss: 32014001 NACRES: NB.24 General descriptionThe Steridilutor® NEO device for liquid transfer kit enables to dilute liquids from open ampoules into a diluent container with septum. For liquid antibiotics, a dilution step is strongly recommended to reduce the concentration of the antimicrobial agent. This will reduce the possibility of binding of the agent to the filter. The liquid transfer kit single needle is a tubing and needle assembly without vent. Small diameter double needle connects test product to diluent. The assembly is to be used for difficult to dissolve powders, dilution and pooling of viscous products in vials as well as antibiotics. The diluted products are subsequently tested with suitable Steritest® Neo canister.ApplicationSteridilutor® NEO devices for liquid transfer is used for the transfer of liquids from ampoules or vials to a diluent vial with septum pooling. The tubing and needle assembly is also used to dilute and pool products in vials.Legal InformationSTERIDILUTOR is a registered trademark of Merck KGaA, Darmstadt, Germany
STERITEST is a registered trademark of Merck KGaA, Darmstadt, GermanyПараметрыQuality Level 400, material Nylon 66 adapter (for needle), PVC tubing, stainless steel (for needle) Agency/Method EP (2.6.1), JP (4.06), USP 71 sterility sterile; -irradiated Торговая марка Steridilutor® packaging pkg of 10 blisters per box, Single packed application(s) sterility testing: suitable input sample type pharmaceutical(s) Featured Industry Pharmaceutical shipped in ambient Узнать цену -
Steridilutor® NEO Device TZVC00010
eCl@ss: 32014001 NACRES: NB.24 General descriptionThe Steridilutor® NEO device with expansion chamber is a tubing and needle assembly for difficult to dissolve powders, for dilution of super-potent antibiotics and pool products in vials. Pure products (solid or liquid) are difficult to rinse and residuals from products might be a major inhibitory factor in sterility testing. In the case of powders, a good dissolution is required to avoid any possible aggregate. A dilution step is strongly recommended for liquid antibiotics to reduce the concentration of the antimicrobial agent. This will reduce the possibility of binding of the agent to the filter. The expansion chamber vents residual vacuum or pressure from the vials without after-drip or contamination risk. The small diameter double needle connects test products with the diluent. The diluted product is subsequently filtered with suitable Steritest® NEO devices.ApplicationThe Steridilutor® NEO Device with expansion chamber is used for the dilution of powders and super-potent antibiotics and to pool products in vials. The expansion chamber enables the venting of diluent container.Legal InformationSTERIDILUTOR is a registered trademark of Merck KGaA, Darmstadt, Germany
STERITEST is a registered trademark of Merck KGaA, Darmstadt, GermanyПараметрыQuality Level 400, material Nylon 66 adapter (for needle), PVC tubing, stainless steel (for needle) Agency/Method EP (2.6.1), JP (4.06), USP 71 sterility sterile; -irradiated Торговая марка Steridilutor® packaging pkg of 10 blisters per box, Single packed application(s) sterility testing: suitable input sample type pharmaceutical(s) Featured Industry Pharmaceutical shipped in ambient Узнать цену -
Steridilutor® NEO Device TZV000010
eCl@ss: 32014001 NACRES: NB.24 General descriptionThe Steridilutor® NEO Device without expansion chamber is a tubing and needle assembly for difficult to dissolve powders, for dilution of super-potent antibiotics and pool products in vials. Pure products (solid or liquid) are difficult to rinse and residuals from products might be a major inhibitory factor in sterility testing. In the case of powders, a good dissolution is required to avoid any possible aggregate. A dilution step is strongly recommended for super potent antibiotics to reduce the concentration of the antimicrobial agent. This will reduce the possibility of binding of the agent to the filter. The small diameter double needle connects test products to the diluent. The diluted product is subsequently filtered with suitable Steritest® NEO devices.ApplicationThe Steridilutor® NEO Device without expansion chamber is used for difficult to dissolve powders, dilution of viscous products and pool products in vials. It helps for faster, easier and safer sterility testing.Legal InformationSTERIDILUTOR is a registered trademark of Merck KGaA, Darmstadt, Germany
STERITEST is a registered trademark of Merck KGaA, Darmstadt, GermanyПараметрыQuality Level 400, material Nylon 66 adapter (for needle), PVC tubing, stainless steel (for needle) Agency/Method EP (2.6.1), JP (4.06), USP 71 sterility sterile; -irradiated Торговая марка Steridilutor® packaging pkg of 10 blisters per box, Single packed application(s) sterility testing: suitable input sample type pharmaceutical(s) Featured Industry Pharmaceutical shipped in ambient Узнать цену -
Steritest® ampoule breaker end cap with seal SYMBECS01
General descriptionSteritest® ampoule breaker replacement kit containing end cap with seal.ApplicationAccessories for Streamlining Your Workflow and Increasing Safety during sterility testing.Legal InformationSTERITEST is a registered trademark of Merck KGaA, Darmstadt, GermanyПараметрыAgency/Method EP (2.6.1), JP (4.06), USP (71) Торговая марка Steritest® application(s) sterility testing: suitable input pharmaceutical(s) Featured Industry Pharmaceutical compatibility for use with Steritest® Symbio pump shipped in ambient Узнать цену -
Steritest® carrying trays SYMBCAN08
eCl@ss: 32014001 NACRES: NB.24 General descriptionSteritest® carrying trays are the accessories that can be used with Steritest® NEO devices. A single carrying tray secures up to 5 canisters in an upright position at the end of the sterility test, facilitating safe transport of the canisters from the test environment to the incubator. It enables the user to visually inspect all 5 canisters at once by gently swirling the carrying tray during intermediate and final readings of the sterility test. The combination of 4 Steritest® carrying trays and a Steritest® rack enables the user to safely transport 20 media-filled canisters at once. The Steritest® canisters carrying trays and Steritest® rack can remain in the incubator.ApplicationSteritest® carrying trays are used to streamline your workflow and increase safety during laboratory filtration and sterility testing.Legal InformationSTERITEST is a registered trademark of Merck KGaA, Darmstadt, GermanyПараметрыmaterial polyphenylsulfone (PPSU) Agency/Method EP 2.6.1, JP 4.06, USP 71 Торговая марка Steritest® packaging pkg of (8 trays per pack) application(s) sterility testing: suitable input sample type pharmaceutical(s) Featured Industry Pharmaceutical compatibility for use with Steritest® NEO Devices, for use with Steritest® Symbio Pump, standard for VHP (Autoclavable) shipped in ambient Узнать цену -
Steritest® Glass Ampoule Breaker SYMBABR01
eCl@ss: 32014001 NACRES: NB.24 General descriptionThe STERITEST® Glass Ampoule Breaker is an accessory of STERITEST® Symbio pumps. The vertical design prevents glass particles and droplets to fall on the bench. The stable stand allows flexible placement in the testing environment. Glass tops of up to 60 ampoules can be collected in the container. The ampoule tops can be directly and safely emptied into the STERITEST® blister for disposal. This accessory is autoclavable and resistant to vaporized hydrogen peroxide (VHP) and peracetic acid decontamination cycles in isolators.ApplicationSTERITEST® Glass Ampoule Breaker is used to safely open the glass ampoules (with or without Pre-scored necks). This accessory streamlines the workflow and increases safety during laboratory filtration and sterility testing.Legal InformationSTERITEST is a registered trademark of Merck KGaA, Darmstadt, GermanyПараметрыmaterial 316L stainless steel , polyphenylsulfone (PPSU) , silicone Agency/Method EP 2.6.1, JP 4.06, USP 71 Торговая марка Steritest® application(s) sample preparation: suitable (laboratory filtration), sterility testing: suitable H 169 mm (6.65 in.) W 121 mm (4.76 in.) depth 130 mm (5.12 in.) weight 2.0 kg (4.4 lb) input sample type pharmaceutical(s) Featured Industry Pharmaceutical compatibility for use with Steritest® Symbio Pump, standard for VHP shipped in ambient Узнать цену -
Steritest® NEO Device TZHALA210
eCl@ss: 32014001 NACRES: NB.24 General descriptionDevice Configuration: 2 canisters
Steritest® NEO Device is a membrane filtration device for sterility testing of filterable pharmaceutical products. The device simplifies every aspect of testing, from handling to traceability. The closed system minimizes false positives and offers the highest levels of quality and reliability. This device ensures that pharmaceutical products are never exposed to the environment during the testing process. This test system offers an optimized and fully regulatory compliant testing process when used with the Steritest® Symbio pump, specific accessories and high-quality culture media and rinsing fluids. The device includes a single needle for easy access to ampoules and a separate vent needle. A single needle adapter enables easy access to collapsible bags. The canisters with blue base indicate mixed cellulose ester (MCE) membrane, which provides an optimal filtration flow rate for standard products.ApplicationThe Steritest® NEO Device is used for sterility testing of large volume parenterals and synthetic drugs without antimicrobial activity.Legal InformationMF-Millipore is a registered trademark of Merck KGaA, Darmstadt, Germany
STERITEST is a registered trademark of Merck KGaA, Darmstadt, GermanyПараметрыQuality Level 400 material Nylon 66 adapter (for needle), PVC tubing (double lumen), mixed cellulose esters (MCE) membrane, plain filter, stainless steel (for needle), styrene-acrylonitrile (SAN) (for canister) Agency/Method EP (2.6.1), JP (4.06), USP 71 sterility sterile; -irradiated Торговая марка Steritest® packaging pkg of 10 blisters per box, Single packed parameter 3.1 bar max. inlet pressure (45 psi) at 25 °C, 45 °C max. temp. application(s) sterility testing: suitable tubing L 850 mm color blue Canister Base matrix MF-Millipore® pore size 0.45 µm pore size input liquid
sample type pharmaceutical(s)test parameters sample volume: 120 mL (graduation marks at 25, 50, 75 and 100 mL) Featured Industry Pharmaceutical shipped in ambient
Safety InformationWGK Germany WGK 2 1 228,31 € / 119 862 ₽Получить предложение -
Steritest® NEO Device TZHASV210
eCl@ss: 32014001 NACRES: NB.24 General descriptionDevice Configuration: 2 canisters
Steritest® NEO is a membrane filtration device for sterility testing of filterable pharmaceutical products. The device simplifies every aspect of testing, from handling to traceability. The closed system ensures that pharmaceutical products are never exposed to the environment during the testing process, minimizes false positives, and offers the highest levels of quality and reliability. This test system offers an optimized and fully regulatory compliant testing process when used with the Steritest® Symbio pump, specific accessories and high-quality culture media and rinsing fluids. The device is provided with a small diameter double needle adapter for small vials with septa. The blue canisters indicate mixed cellulose ester (MCE) membrane, which provides an optimal filtration flow rate for standard products.ApplicationThe Steritest® NEO Device is used for sterility testing of small volume parenterals and synthetic drugs without antimicrobial activity.Legal InformationMF-Millipore is a registered trademark of Merck KGaA, Darmstadt, Germany
STERITEST is a registered trademark of Merck KGaA, Darmstadt, GermanyПараметрыQuality Level 400 material Nylon 66 adapter (for needle), PVC tubing (double lumen), mixed cellulose esters (MCE) membrane, plain filter, stainless steel (for needle), styrene-acrylonitrile (SAN) (for canister) Agency/Method EP (2.6.1), JP (4.06), USP 71 sterility sterile; -irradiated Торговая марка Steritest® packaging pkg of 10 blisters per box, Single packed parameter 3.1 bar max. inlet pressure (45 psi) at 25 °C, 45 °C max. temp. application(s) sterility testing: suitable tubing L 850 mm color blue Canister Base matrix MF-Millipore® pore size 0.45 µm pore size input sample type pharmaceutical(s)
liquidtest parameters sample volume: 120 mL (graduation marks at 25, 50, 75 and 100 mL) Featured Industry Pharmaceutical shipped in ambient
Safety InformationWGK Germany WGK 2 Узнать цену -
Steritest® NEO Device TZHALV210
eCl@ss: 32014001 NACRES: NB.24 General descriptionThe STERITEST<GammabestrahlungApplicationThe Steritest® NEO Device is used for sterility testing of large volume parenterals and synthetic drugs without antimicrobial activity.Legal InformationMF-Millipore is a registered trademark of Merck KGaA, Darmstadt, Germany
STERITEST is a registered trademark of Merck KGaA, Darmstadt, GermanyПараметрыQuality Level 400 material Nylon 66 adapter (for needle), PVC tubing (double lumen), mixed cellulose esters (MCE) membrane, plain filter, stainless steel (for needle), styrene-acrylonitrile (SAN) (for canister) Agency/Method EP (2.6.1), JP (4.06), USP 71 sterility sterile; -irradiated Торговая марка Steritest® packaging pkg of 10 blisters per box, Single packed parameter 3.1 bar max. inlet pressure (45 psi) at 25 °C, 45 °C max. temp. application(s) sterility testing: suitable tubing L 850 mm color blue Canister Base matrix MF-Millipore® pore size 0.45 µm pore size input liquid
sample type pharmaceutical(s)test parameters sample volume: 120 mL (graduation marks at 25, 50, 75 and 100 mL) Featured Industry Pharmaceutical shipped in ambient
Safety InformationWGK Germany WGK 2 Узнать цену -
Steritest® NEO Device TZHVAB210
eCl@ss: 32014001 NACRES: NB.24 General descriptionDevice Configuration: 2 canisters
Steritest® NEO Device is a membrane filtration device for sterility testing of filterable pharmaceutical products. The device simplifies every aspect of testing, from handling to traceability. The closed system minimizes false positives, offers the highest levels of quality & reliability, and ensures that pharmaceutical products are not exposed to the environment. This test system offers an optimized and fully regulatory compliant testing process when used with the Steritest® Symbio pump, specific accessories and high-quality culture media and rinsing fluids. A separate vent needle is included for the transfer of the test product, culture media or rinsing buffer. The red canister base indicates low absorption Durapore® polyvinylidene fluoride (PVDF) membrane and specific drain design, to optimize the rising of products that inhibit microbial growth.ApplicationThe Steritest® NEO Device for Liquids Antibiotics is used for sterility testing of antibiotics and products containing antimicrobial agents. The red canister base indicates low absorption Durapore membrane and specific drain design. This optimizes the rinsing of products that inhibit microbial growth.Legal InformationDurapore is a registered trademark of Merck KGaA, Darmstadt, Germany
STERITEST is a registered trademark of Merck KGaA, Darmstadt, GermanyПараметрыQuality Level 400 material Nylon 66 adapter (for needle), PVC tubing (double lumen), PVDF membrane, plain filter, stainless steel (for needle), styrene-acrylonitrile (SAN) (for canister) Agency/Method EP (2.6.1), JP (4.06), USP 71 sterility sterile; -irradiated Торговая марка Steritest® packaging pkg of 10 blisters per box, Single packed parameter 3.1 bar max. inlet pressure (45 psi) at 25 °C, 45 °C max. temp. application(s) sterility testing: suitable tubing L 850 mm color red Canister Base matrix Durapore® pore size 0.45 µm pore size input sample type pharmaceutical(s) test parameters sample volume: 120 mL (graduation marks at 25, 50, 75 and 100 mL) Featured Industry Pharmaceutical shipped in ambient 1 050,80 € / 102 540 ₽Получить предложение -
Steritest® NEO Device TZHVSL210
eCl@ss: 32014001 NACRES: NB.24 General descriptionDevice Configuration: 2 canisters
Steritest® NEO Device is a membrane filtration device for sterility testing of filterable pharmaceutical products. The device simplifies every aspect of testing, from handling to traceability. The closed system minimizes false positives and offers the highest levels of quality and reliability, ensuring that pharmaceutical products are never exposed to the environment during the testing process. This test system offers an optimized and fully regulatory compliant testing process, when used with the Steritest® Symbio pump, specific accessories and high-quality culture media and rinsing fluids. The canister connections and reinforced base structure provide better resistance to pressure. The single needle adapter is used for products in vials or ampoules. A separate vent needle is included for the transfer of the test product, culture media or rinsing buffer. The canisters come with green canister base indicating increased chemical compatibility with solvents due to Durapore® Poly vinylidene fluoride (PVDF) membrane and specific canister polymer (nylon). This optimizes the chemical compatibility of products dissolved in solvents.ApplicationThe Steritest® NEO Device is used for sterility testing of products dissolved in solvents (such as creams, ointments and veterinary injectables), requiring increased chemical compatibility.Legal InformationDurapore is a registered trademark of Merck KGaA, Darmstadt, Germany
STERITEST is a registered trademark of Merck KGaA, Darmstadt, GermanyПараметрыQuality Level 400 material Nylon (for canister), Nylon 66 adapter (for needle), PVC tubing (double lumen), PVDF membrane, plain filter, stainless steel (for needle) Agency/Method EP (2.6.1), JP (4.06), USP 71 sterility sterile; -irradiated Торговая марка Steritest® packaging pkg of 10 blisters per box, Single packed parameter 3.1 bar max. inlet pressure (45 psi) at 25 °C, 45 °C max. temp. application(s) sterility testing: suitable tubing L 850 mm color green Canister Base matrix Durapore® pore size 0.45 µm pore size input sample type pharmaceutical(s)
solvent(s)test parameters sample volume: 120 mL (graduation marks at 25, 50, 75 and 100 mL) Featured Industry Pharmaceutical shipped in ambient 1 226,32 € / 119 668 ₽Получить предложение -
Steritest® NEO Device TZHAPC210
eCl@ss: 32014001 NACRES: NB.24 General descriptionDevice Configuration: 2 canisters
Steritest® NEO is a membrane filtration device for sterility testing of filterable pharmaceutical products. The device simplifies every aspect of testing, from handling to traceability. The closed system minimizes false positives and offers the highest levels of quality and reliability. This device ensures that pharmaceutical products are never exposed to the environment during the testing process. This test system offers an optimized and fully regulatory compliant testing process when used with the Steritest® Symbio pump, specific accessories and high-quality culture media and rinsing fluids. The non-coring needle adapter with aperture on side of needle adapter minimizes the blockage. A separate vent needle is included for the transfer of the test product, culture media or rinsing buffer. The canisters with blue base indicate mixed cellulose ester (MCE) membrane, which provides an optimal filtration flow rate for standard products.ApplicationThe Steritest® NEO Device is used for sterility testing of liquids in plastic containers, without antimicrobial agents.Legal InformationMF-Millipore is a registered trademark of Merck KGaA, Darmstadt, Germany
STERITEST is a registered trademark of Merck KGaA, Darmstadt, GermanyПараметрыQuality Level 400 material Nylon 66 adapter (for needle), PVC tubing (double lumen), mixed cellulose esters (MCE) membrane, plain filter, stainless steel (for needle), styrene-acrylonitrile (SAN) (for canister) Agency/Method EP (2.6.1), JP (4.06), USP 71 sterility sterile; -irradiated Торговая марка Steritest® packaging pkg of 10 blisters per box, Single packed parameter 3.1 bar max. inlet pressure (45 psi) at 25 °C, 45 °C max. temp. application(s) sterility testing: suitable tubing L 850 mm color blue Canister Base matrix MF-Millipore® pore size 0.45 µm pore size input liquid
sample type pharmaceutical(s)test parameters sample volume: 120 mL (graduation marks at 25, 50, 75 and 100 mL) Featured Industry Pharmaceutical shipped in ambient Узнать цену -
Steritest® NEO Device TZHADV210
eCl@ss: 32014001 NACRES: NB.24 General descriptionDevice Configuration: 2 canisters
Steritest® NEO Device is a membrane filtration device for sterility testing of filterable pharmaceutical products. The device simplifies every aspect of testing, from handling to traceability. The closed system ensures that pharmaceutical products are never exposed to the environment during the testing process. This minimizes false positives and offers the highest levels of quality and reliability. This test system offers an optimized and fully regulatory compliant testing process, when used with the Steritest® Symbio pump, specific accessories and high-quality culture media and rinsing fluids. A small diameter double needle adapter is used for small vials with septa. The blue based canisters indicate mixed cellulose esters (MCE) membrane, which provides an optimal filtration flow rate for standard products.ApplicationThe Steritest® NEO Device is used for sterility testing of soluble powders in vials, without antimicrobial agents. The device simultaneously dissolves/dilutes the sample in sterile diluent and transfers the resulting solution to canisters for further filtration.Legal InformationMF-Millipore is a registered trademark of Merck KGaA, Darmstadt, Germany
STERITEST is a registered trademark of Merck KGaA, Darmstadt, GermanyПараметрыQuality Level 400 material Nylon 66 adapter (for needle), PVC tubing (double lumen), mixed cellulose esters (MCE) membrane, plain filter, stainless steel (for needle), styrene-acrylonitrile (SAN) (for canister) Agency/Method EP (2.6.1), JP (4.06), USP 71 sterility sterile; -irradiated Торговая марка Steritest® packaging pkg of 10 blisters per box, Single packed parameter 3.1 bar max. inlet pressure (45 psi) at 25 °C, 45 °C max. temp. application(s) sterility testing: suitable tubing L 850 mm color blue Canister Base matrix MF-Millipore® pore size 0.45 µm pore size input liquid
sample type pharmaceutical(s)test parameters sample volume: 120 mL (graduation marks at 25, 50, 75 and 100 mL) Featured Industry Pharmaceutical shipped in ambient
Safety InformationWGK Germany WGK 2 Узнать цену -
Steritest® NEO Device TZHVDV210
eCl@ss: 32014001 NACRES: NB.24 General descriptionDevice Configuration: 2 canisters
Steritest® NEO is a membrane filtration device for sterility testing of filterable pharmaceutical products. The device simplifies every aspect of testing, from handling to traceability. The closed system minimizes false positives and offers the highest levels of quality and reliability. This device ensures that pharmaceutical products are never exposed to the environment during the testing process. This test system offers an optimized and fully regulatory compliant testing process when used with the Steritest® Symbio pump, specific accessories and high-quality culture media and rinsing fluids. The device simultaneously dissolves/dilutes in sterile diluents and filters the resulting solution. A small diameter double needle adapter is used for small vials with septa. The red canister base indicates low absorption Durapore® hydrophilic Poly vinylidene fluoride (PVDF) membrane and specific drain design. This optimizes the rising of products that inhibit microbial growth.ApplicationThe Steritest® NEO Device is used for sterility testing of soluble powders in vials and products with antimicrobial activity that require dilution or dissolution.Legal InformationDurapore is a registered trademark of Merck KGaA, Darmstadt, Germany
STERITEST is a registered trademark of Merck KGaA, Darmstadt, GermanyПараметрыQuality Level 400, material Nylon 66 adapter (for needle), PVC tubing (double lumen), PVDF membrane, plain filter, stainless steel (for needle), styrene-acrylonitrile (SAN) (for canister) Agency/Method EP (2.6.1), JP (4.06), USP 71 sterility sterile; -irradiated Торговая марка Steritest® packaging pkg of 10 blisters per box, Single packed parameter 3.1 bar max. inlet pressure (45 psi) at 25 °C, 45 °C max. temp. application(s) sterility testing: suitable tubing L 850 mm color red Canister Base matrix Durapore® pore size 0.45 µm pore size input sample type pharmaceutical(s) test parameters sample volume: 120 mL (graduation marks at 25, 50, 75 and 100 mL) Featured Industry Pharmaceutical shipped in ambient Узнать цену -
Steritest® NEO Device TZHVSV210
eCl@ss: 32014001 NACRES: NB.24 General descriptionDevice Configuration: 2 canisters
Steritest® NEO Device is a membrane filtration device for sterility testing of filterable pharmaceutical products. The device simplifies every aspect of testing, from handling to traceability. The closed system minimizes false positives and offers the highest levels of quality and reliability. This device ensures that pharmaceutical products are never exposed to the environment during the testing process. This test system offers an optimized and fully regulatory compliant testing process, when used with the Steritest® Symbio pump, specific accessories and high-quality culture media and rinsing fluids. The device comes with vented double needle for small vials with septum. The red canister base indicates low absorption Durapore® hydrophilic Poly vinylidene fluoride (PVDF) membrane and specific drain design. This optimizes the rinsing of products that inhibit microbial growth.ApplicationThe Steritest® NEO Device for liquids in small vials is used for sterility testing of antibiotics, products containing antimicrobial agents.Legal InformationDurapore is a registered trademark of Merck KGaA, Darmstadt, Germany
STERITEST is a registered trademark of Merck KGaA, Darmstadt, GermanyПараметрыQuality Level 400, material Nylon 66 adapter (for needle), PVC tubing (double lumen), PVDF membrane, plain filter, stainless steel (for needle), styrene-acrylonitrile (SAN) (for Canister) Agency/Method EP (2.6.1), JP (4.06), USP 71 sterility sterile; -irradiated Торговая марка Steritest® packaging pkg of 10 blisters per box, Single packed parameter 3.1 bar max. inlet pressure (45 psi) at 25 °C, 45 °C max. temp. application(s) sterility testing: suitable tubing L 850 mm color red Canister Base matrix Durapore® pore size 0.45 µm pore size input liquid
sample type pharmaceutical(s)test parameters sample volume: 120 mL (graduation marks at 25, 50, 75 and 100 mL) Featured Industry Pharmaceutical shipped in ambient Узнать цену -
Steritest® NEO Device TZHAMD210
eCl@ss: 32014001 NACRES: NB.24 General descriptionDevice Configuration: 2 canisters
Steritest® NEO Device is a membrane filtration device for sterility testing of filterable pharmaceutical products. The device simplifies every aspect of testing, from handling to traceability. The closed system ensures that pharmaceutical products are never exposed to the environment during the testing process. This minimizes false positives and offers the highest levels of quality and reliability. This test system offers an optimized and fully regulatory compliant testing process, when used with the Steritest® Symbio pump, specific accessories and high-quality culture media and rinsing fluids. The Steritest® NEO Device for medical devices provides three adapters: male Luer, female Luer or single needle allow connection to a variety of test devices. A separate vent needle is used for the transfer of culture media or rinse buffer. The Steritest® NEO Device for medical devices can be used with Novaseptum® for sterile sampling devices. The blue canister base indicates mixed cellulose esters (MCE) membrane. This membrane provides an optimal filtration flow rate for standard products.ApplicationSteritest® NEO Device for medical device and collapsible bags is used for sterility testing of medical devices, collapsible bags and products without antimicrobial agents.Legal InformationMF-Millipore is a registered trademark of Merck KGaA, Darmstadt, Germany
NOVASEPTUM is a registered trademark of Millipore AB - Sweden
STERITEST is a registered trademark of Merck KGaA, Darmstadt, GermanyПараметрыQuality Level 400, material Nylon 66 adapter (for needle), PVC tubing (double lumen), mixed cellulose esters (MCE) membrane, plain filter, stainless steel ( for needle), styrene-acrylonitrile (SAN) ( for Canister) Agency/Method EP 2.6.1, JP 4.06, USP 71 sterility sterile; -irradiated Торговая марка Steritest® packaging pkg of 10 blisters per box, Single packed parameter 3.1 bar max. inlet pressure (45 psi) at 25 °C, 45 °C max. temp. application(s) sterility testing: suitable tubing L 850 mm color blue Canister Base matrix MF-Millipore® pore size 0.45 µm pore size input sample type pharmaceutical(s) test parameters sample volume: 120 mL (graduation marks at 25, 50, 75 and 100 mL) Featured Industry Pharmaceutical shipped in ambient Узнать цену -
Steritest® NEO Device TZHASY210
eCl@ss: 32014001 NACRES: NB.24 General descriptionDevice Configuration: 2 canisters
Steritest® NEO Device is a membrane filtration device for sterility testing of filterable pharmaceutical products. The device simplifies every aspect of testing, from handling to traceability. This device ensures that pharmaceutical products are never exposed to the environment during the testing process. The closed system minimizes false positives and offers the highest levels of quality and reliability. This test system offers an optimized and fully regulatory compliant testing process, when used with the Steritest® Symbio pump, specific accessories and high-quality culture media and rinsing fluids. The device comes with vented double needle. The adapter allows for sequential testing of syringe contents and needle surfaces. The system has two blue based canisters with mixed cellulose esters (MCE) membrane, providing an optimal filtration flow rate for standard products.ApplicationThe Steritest® NEO Device for liquids in syringes is used for sterility testing of pre-filled syringes, for products without antimicrobial agents.Legal InformationMF-Millipore is a registered trademark of Merck KGaA, Darmstadt, Germany
STERITEST is a registered trademark of Merck KGaA, Darmstadt, GermanyПараметрыQuality Level 400, material Nylon 66 adapter (for needle), PVC tubing (double lumen), mixed cellulose esters (MCE) membrane, stainless steel (for needle), styrene-acrylonitrile (SAN) (For Canister) Agency/Method EP (2.6.1), JP (4.06), USP 71 sterility sterile; -irradiated Торговая марка Steritest® packaging pkg of 10 blisters per box, Single packed parameter 3.1 bar max. inlet pressure (45 psi) at 25 °C, 45 °C max. temp. application(s) sterility testing: suitable tubing L 850 mm color blue Canister Base matrix MF-Millipore® pore size 0.45 µm pore size input liquid
sample type pharmaceutical(s)test parameters sample volume: 120 mL (graduation marks at 25, 50, 75 and 100 mL) Featured Industry Pharmaceutical shipped in ambient Узнать цену -
Steritest® NEO Device TZHALA205
eCl@ss: 32014001 NACRES: NB.24 General descriptionDevice Configuration: 2 canisters
Steritest® NEO is a membrane filtration device for sterility testing of filterable pharmaceutical products. The device simplifies every aspect of testing, from handling to traceability. The closed system ensures that pharmaceutical products are never exposed to the environment, minimizes false positives, and offers the highest levels of quality and reliability. This test system offers an optimized and fully regulatory compliant testing process when used with the Steritest® Symbio pump, specific accessories and high-quality culture media and rinsing fluids. The device is gamma sterilized and double packed for the quick transfer into sterility testing environments, simplifying decontamination procedures and saving time. A single needle adapter enables an easy access to ampoules or collapsible bags. A separate vent needle is included for the transfer of the test product, culture media or rinsing buffer. The blue based canisters indicate mixed cellulose ester (MCE) membrane, which provides an optimal filtration flow rate for standard products.ApplicationThe Steritest® NEO Device for liquids in ampoules or collapsible bags is used for sterility testing of large volume parenterals and synthetic drugs without antimicrobial activity.Packaging10 ea in 2 bags of 5 blisters per boxLegal InformationMF-Millipore is a registered trademark of Merck KGaA, Darmstadt, Germany
STERITEST is a registered trademark of Merck KGaA, Darmstadt, GermanyПараметрыQuality Level 400, material Nylon 66 adapter (for needle), PVC tubing (double lumen), mixed cellulose esters (MCE) membrane, plain filter, stainless steel (for needle), styrene-acrylonitrile (SAN) (for canister) Agency/Method EP (2.6.1), JP (4.06), USP 71 sterility sterile; -irradiated Торговая марка Steritest® packaging pkg of 10 blisters in 2 bags of 5 blisters per box, double packed parameter 3.1 bar max. inlet pressure (45 psi) at 25 °C, 45 °C max. temp. application(s) sterility testing: suitable tubing L 850 mm color blue Canister Base matrix MF-Millipore® pore size 0.45 µm pore size input sample type pharmaceutical(s)
liquidtest parameters sample volume: 120 mL (graduation marks at 25, 50, 75 and 100 mL) Featured Industry Pharmaceutical shipped in ambient
Safety InformationWGK Germany WGK 2 Узнать цену -
Steritest® NEO Device TZHVLV210
eCl@ss: 32014001 NACRES: NB.24 General descriptionDevice Configuration: 2 canisters
Steritest® NEO is a membrane filtration device for sterility testing of filterable pharmaceutical products. The device simplifies every aspect of testing, from handling to traceability. The closed system minimizes false positives and offers the highest levels of quality and reliability. This device ensures that pharmaceutical products are never exposed to the environment during the testing process. This test system offers an optimized and fully regulatory compliant testing process when used with the Steritest® Symbio pump, specific accessories and high-quality culture media and rinsing fluids. A vented needle adapter vents and transfers the test product from large volume containers with a septum to the Steritest® NEO device. The red canister base indicates low absorption Durapore® hydrophilic Poly vinylidene fluoride (PVDF) membrane and specific drain design. This optimizes the rising of products that inhibit microbial growth. The canister capacity of 120 mL allows to test larger volumes.ApplicationThe Steritest® NEO Device for liquids in large vials is used for sterility testing of large volume of products with antimicrobial activity.Legal InformationDurapore is a registered trademark of Merck KGaA, Darmstadt, Germany
STERITEST is a registered trademark of Merck KGaA, Darmstadt, GermanyПараметрыQuality Level 400, material Nylon 66 adapter (for needle), PVC tubing (double lumen), PVDF membrane, plain filter, stainless steel (for needle), styrene-acrylonitrile (SAN) (for canister) Agency/Method EP (2.6.1), JP (4.06), USP 71 sterility sterile; -irradiated Торговая марка Steritest® packaging pkg of 10 blisters per box, Single packed parameter 3.1 bar max. inlet pressure (45 psi) at 25 °C, 45 °C max. temp. application(s) sterility testing: suitable tubing L 850 mm color red Canister Base matrix Durapore® pore size 0.45 µm pore size input liquid
sample type pharmaceutical(s)test parameters sample volume: 120 mL (graduation marks at 25, 50, 75 and 100 mL) Featured Industry Pharmaceutical shipped in ambient Узнать цену -
Steritest® NEO Device TZHADA210
eCl@ss: 32014001 NACRES: NB.24 General descriptionDevice Configuration: 2 canisters
Steritest® NEO Device is a membrane filtration device for sterility testing of filterable pharmaceutical products. The device simplifies every aspect of testing, from handling to traceability. The closed system minimizes false positives, offers the highest levels of quality and reliability, and ensures that pharmaceutical products are never exposed to the environment during the testing process. This test system offers an optimized and fully regulatory compliant testing process, when used with the Steritest® Symbio pump, specific accessories and high-quality culture media and rinsing fluids. The device has vented double needle and simultaneously dissolves/dilutes the sample in sterile diluent and transfers the resulting solution to canisters for further filtration. The blue based canisters indicate mixed cellulose esters (MCE) membrane, which provides an optimal filtration flow rate for standard products.ApplicationThe Steritest® NEO Device is used for sterility testing of soluble powders in ampoules, without antimicrobial agent. The device simultaneously dilutes and transfers the test products to the canister set.Legal InformationMF-Millipore is a registered trademark of Merck KGaA, Darmstadt, Germany
STERITEST is a registered trademark of Merck KGaA, Darmstadt, GermanyПараметрыQuality Level 400, material Nylon 66 adapter (for needle), PVC tubing (double lumen), mixed cellulose esters (MCE) membrane, plain filter, stainless steel (for needle), styrene-acrylonitrile (SAN) (for canister) Agency/Method EP (2.6.1), JP (4.06), USP 71 sterility sterile; -irradiated Торговая марка Steritest® packaging pkg of 10 blisters per box, Single packed parameter 3.1 bar max. inlet pressure (45 psi) at 25 °C, 45 °C max. temp. application(s) sterility testing: suitable tubing L 850 mm color blue Canister Base matrix MF-Millipore® pore size 0.45 µm pore size input sample type pharmaceutical(s) test parameters sample volume: 120 mL (graduation marks at 25, 50, 75 and 100 mL) Featured Industry Pharmaceutical shipped in ambient
Safety InformationWGK Germany WGK 2 Узнать цену -
Steritest® NEO Device TZHASV205
eCl@ss: 32014001 NACRES: NB.24 General descriptionDevice Configuration: 2 canisters
Steritest® NEO is a membrane filtration device for sterility testing of filterable pharmaceutical products. The device simplifies every aspect of testing, from handling to traceability. The closed system minimizes false positives, offers the highest levels of quality & reliability, and ensures that pharmaceutical products are never exposed to the environment during the testing process. This test system offers an optimized and fully regulatory compliant testing process when used with the Steritest® Symbio pump, specific accessories and high-quality culture media and rinsing fluids. The device is gamma sterilized and double packed for the quick transfer into sterility testing environments, simplifying decontamination procedures and saving time. The Steritest® NEO Double Packed device contains a small diameter double needle adapter for small vials with septum. The blue canister base indicates mixed esters of cellulose membrane. This membrane provides an optimal filtration flow rate for standard products.ApplicationSteritest® NEO Device for liquids in small vials is used for sterility testing of small volume parenterals and synthetic drugs without antimicrobial activity.Packaging10 ea in 2 bags of 5 blisters per boxLegal InformationMF-Millipore is a registered trademark of Merck KGaA, Darmstadt, Germany
STERITEST is a registered trademark of Merck KGaA, Darmstadt, GermanyПараметрыQuality Level 400, material Nylon 66 adapter (for needle), PVC tubing (double lumen), mixed cellulose esters (MCE) membrane, plain filter, stainless steel (for needle), styrene-acrylonitrile (SAN) (for canister) Agency/Method EP (2.6.1), JP (4.06), USP 71 sterility sterile; -irradiated Торговая марка Steritest® packaging pkg of 10 blisters in 2 bags of 5 blisters per box, Double packed parameter 3.1 bar max. inlet pressure (45 psi) at 25 °C, 45 °C max. temp. application(s) sterility testing: suitable tubing L 850 mm color blue Canister Base matrix MF-Millipore® pore size 0.45 µm pore size input sample type pharmaceutical(s)
liquidtest parameters sample volume: 120 mL (graduation marks at 25, 50, 75 and 100 mL) Featured Industry Pharmaceutical shipped in ambient Узнать цену -
Steritest® NEO Device TZHALV205
eCl@ss: 32014001 NACRES: NB.24 General descriptionDevice Configuration: 2 canisters
Steritest® NEO Device is a membrane filtration device for sterility testing of filterable pharmaceutical products. The device simplifies every aspect of testing, from handling to traceability. The closed system minimizes false positives and offers the highest levels of quality and reliability. This device ensures that pharmaceutical products are never exposed to the environment during the testing process. This test system offers an optimized and fully regulatory compliant testing process, when used with the Steritest® Symbio pump, specific accessories and high-quality culture media and rinsing fluids. The device is gamma sterilized and double packed for the quick transfer into sterility testing environments, simplifying decontamination procedures and saving time. A vented needle adapter vents and transfers the test product from large volume containers with a septum to the Steritest® NEO devices. The blue based canisters indicate mixed cellulose esters (MCE) membrane, which provides an optimal filtration flow rate for standard products.ApplicationThe Steritest® NEO Device is used for sterility testing of liquids in large vials (double packed), which includes large volume parenterals and synthetic drugs, without antimicrobial agent.Packaging10 ea in 2 bags of 5 blisters per boxLegal InformationMF-Millipore is a registered trademark of Merck KGaA, Darmstadt, Germany
STERITEST is a registered trademark of Merck KGaA, Darmstadt, GermanyПараметрыQuality Level 400, material Nylon 66 adapter (for needle), PVC tubing (double lumen), mixed cellulose esters (MCE) membrane, plain filter, stainless steel (for needle), styrene-acrylonitrile (SAN) (for canister) Agency/Method EP (2.6.1), JP (4.06), USP 71 sterility sterile; -irradiated Торговая марка Steritest® packaging pkg of 10 blisters in 2 bags of 5 blisters per box, Double packed parameter 3.1 bar max. inlet pressure (45 psi) at 25 °C, 45 °C max. temp. application(s) sterility testing: suitable tubing L 850 mm color blue Canister Base matrix MF-Millipore® pore size 0.45 µm pore size input liquid
sample type pharmaceutical(s)test parameters sample volume: 120 mL (graduation marks at 25, 50, 75 and 100 mL) Featured Industry Pharmaceutical shipped in ambient
Safety InformationWGK Germany WGK 2 Узнать цену -
Steritest® NEO Device TZHVAB205
eCl@ss: 32014001 NACRES: NB.24 General descriptionDevice Configuration: 2 canisters
Steritest® NEO is a membrane filtration device for sterility testing of filterable pharmaceutical products. The device simplifies every aspect of testing, from handling to traceability. The closed system minimizes false positives and offers the highest levels of quality and reliability. This device ensures that pharmaceutical products are never exposed to the environment during the testing process. This test system offers an optimized and fully regulatory compliant testing process when used with the Steritest® Symbio pump, specific accessories and high-quality culture media and rinsing fluids. The Steritest® NEO Double Packed Device for Liquids Antibiotics is gamma sterilized and double packed for the quick transfer into sterility testing environments, simplifying decontamination procedures and saving time. A separate vent needle is included for the transfer of the test product, culture media or rinsing buffer. The red canister base indicates low absorption. Durapore® hydrophilic Poly vinylidene fluoride (PVDF) membrane and specific drain design. This optimizes the rinsing of products that inhibit microbial growth.ApplicationThe Steritest® NEO Device for Liquids Antibiotics is used for sterility testing of antibiotics and products containing antimicrobial agents.Legal InformationDurapore is a registered trademark of Merck KGaA, Darmstadt, Germany
STERITEST is a registered trademark of Merck KGaA, Darmstadt, GermanyПараметрыQuality Level 400, material Nylon 66 adapter (for needle), PVC tubing (double lumen), PVDF membrane, plain filter, stainless steel (for needle), styrene-acrylonitrile (SAN) (for canister) Agency/Method EP (2.6.1), JP (4.06), USP 71 sterility sterile; -irradiated Торговая марка Steritest® packaging pkg of 10 blisters in 2 bags of 5 blisters per box, Double packed parameter 3.1 bar max. inlet pressure (45 psi) at 25 °C, 45 °C max. temp. application(s) sterility testing: suitable tubing L 850 mm color red Canister Base matrix Durapore® pore size 0.45 µm pore size input sample type pharmaceutical(s) test parameters sample volume: 120 mL (graduation marks at 25, 50, 75 and 100 mL) Featured Industry Pharmaceutical shipped in ambient Узнать цену -
Steritest® NEO Device TZHVDV205
eCl@ss: 32014001 General descriptionDevice configuration: 2 canisters
Steritest® NEO is a membrane filtration device for sterility testing of filterable pharmaceutical products. The device simplifies every aspect of testing, from handling to traceability. The closed system ensures that pharmaceutical products are never exposed to the environment, minimizes false positives, and offers the highest levels of quality & reliability. This test system offers an optimized and fully regulatory compliant testing process when used with the Steritest® Symbio pump, specific accessories and high-quality culture media and rinsing fluids. The device is gamma sterilized and double packed for the quick transfer into sterility testing environments, simplifying decontamination procedures and saving time. The device simultaneously dissolves/dilutes the sample in sterile diluent and transfers the resulting solution to canisters. A small diameter double needle adapter is used for small vials with septum. The red canister base indicates low absorption. Durapore® hydrophilic Poly vinylidene fluoride (PVDF) membrane and specific drain design. This optimizes the rinsing of products that inhibit microbial growth.ApplicationSteritest® NEO Device is used for sterility testing of antibiotics and products with antimicrobial activity that require dilution or dissolution.Legal InformationDurapore is a registered trademark of Merck KGaA, Darmstadt, Germany
STERITEST is a registered trademark of Merck KGaA, Darmstadt, GermanyПараметрыQuality Level 400, material Nylon 66 adapter (for needle), PVC tubing (double lumen), PVDF membrane, plain filter, stainless steel (for needle), styrene-acrylonitrile (SAN) (for canister) Agency/Method EP (2.6.1), JP (4.06), USP 71 sterility sterile; -irradiated Торговая марка Steritest® packaging pkg of 10 blisters in 2 bags of 5 blisters per box, Double packed parameter 3.1 bar max. inlet pressure (45 psi) at 25 °C, 45 °C max. temp. application(s) sterility testing: suitable tubing L 850 mm color red Canister Base matrix Durapore® pore size 0.45 µm pore size input sample type pharmaceutical(s) test parameters sample volume: 120 mL (graduation marks at 25, 50, 75 and 100 mL) Featured Industry Pharmaceutical shipped in ambient Узнать цену -
Steritest® NEO Device TZHVSV205
General descriptionDevice Configuration: 2 canisters
Steritest® NEO is a membrane filtration device for sterility testing of filterable pharmaceutical products. The device simplifies every aspect of testing, from handling to traceability. The closed system minimizes false positives and offers the highest levels of quality and reliability. This device ensures that pharmaceutical products are never exposed to the environment during the testing process. This test system offers an optimized and fully regulatory compliant testing process when used with the Steritest® Symbio pump, specific accessories and high-quality culture media and rinsing fluids. The Steritest® NEO Double Packed Device for liquids in small vials is gamma sterilized and double packed for the quick transfer into sterility testing environments, simplifying decontamination procedures and saving time. The device contains a small diameter double needle adapter for small vials with septum. The red canister base indicates low absorption. Durapore® hydrophilic Poly vinylidene fluoride (PVDF) membrane and specific drain design. This optimizes the rinsing of products that inhibit microbial growth.ApplicationSteritest® NEO Device for liquids in small vials is used for sterility testing of small volume parenterals of products with antimicrobial activity.Legal InformationDurapore is a registered trademark of Merck KGaA, Darmstadt, Germany
STERITEST is a registered trademark of Merck KGaA, Darmstadt, GermanyПараметрыQuality Level 400, material Nylon 66 adapter (for needle), PVC tubing (double lumen), PVDF membrane, plain filter, stainless steel (for needle), styrene-acrylonitrile (SAN) (for canister) Agency/Method EP (2.6.1), JP (4.06), USP (71) sterility sterile; -irradiated Торговая марка Steritest® packaging pkg of 10 blisters in 2 bags of 5 blisters per box, Double packed application(s) sterility testing: suitable color red Canister Base pore size 0.45 µm pore size input pharmaceutical(s)
liquidtest parameters sample volume: 120 mL (graduation marks at 25, 50, 75 and 100 mL) Featured Industry Pharmaceutical shipped in ambient Узнать цену -
Steritest® NEO Device MSP010056
eCl@ss: 32014001 NACRES: NB.24 General descriptionDevice configuration: 2 canisters
Steritest® NEO is a membrane filtration device for sterility testing of filterable pharmaceutical products. The device simplifies every aspect of testing, from handling to traceability. The closed system minimizes false positives and offers the highest levels of quality and reliability. This device ensures that pharmaceutical products are never exposed to the environment during the testing process. This test system offers an optimized and fully regulatory compliant testing process when used with the Steritest® Symbio pump, specific accessories and high-quality culture media and rinsing fluids. A vented needle adapter vents and transfers the test product from large volume containers with a septum to the Steritest® NEO devices. The blue canister base indicates mixed esters of cellulose membrane. This membrane provides an optimal filtration flow rate for standard products.ApplicationThe Steritest® NEO Device for liquids in vials is used for sterility testing of large volume parenterals and synthetic drugs without antimicrobial activity.Legal InformationMF-Millipore is a registered trademark of Merck KGaA, Darmstadt, Germany
STERITEST is a registered trademark of Merck KGaA, Darmstadt, GermanyПараметрыQuality Level 400, material blue base (canister), mixed cellulose esters (MCE) (for membrane filter), plain filter, stainless steel (for needle), styrene-acrylonitrile (SAN) (for canister) Agency/Method EP (2.6.1), JP (4.06), USP (71) sterility sterile; -irradiated Торговая марка Steritest® packaging pkg of 10 blisters per box, Single packed application(s) sterility testing: suitable matrix MF-Millipore® pore size 0.45 µm pore size input pharmaceutical(s) test parameters sample volume: 120 mL (graduation marks at 25, 50, 75 and 100 mL) Featured Industry Pharmaceutical shipped in ambient
Safety InformationWGK Germany WGK 2 Узнать цену -
Steritest® NEO Device TZHVMD210
eCl@ss: 32014001 NACRES: NB.24 General descriptionDevice Configuration: 2 canisters
Steritest® NEO is a membrane filtration device for sterility testing of filterable pharmaceutical products. The device simplifies every aspect of testing, from handling to traceability. The closed system ensures that pharmaceutical products are never exposed to the environment, minimizes false positives, and offers the highest levels of quality and reliability. This test system offers an optimized and fully regulatory compliant testing process when used with the Steritest® Symbio pump, specific accessories and high-quality culture media and rinsing fluids. Steritest® NEO Device for medical devices provides three adapters: male Luer, female Luer or single needle allow connection to a variety of test devices. A separate vent needle is included for the transfer of the test product, culture media or rinse buffer. The Steritest® NEO Device for medical devices can be used with Novaseptum® for sterile sampling devices. The red canister base indicates low absorption. Durapore® hydrophilic Poly vinylidene fluoride (PVDF) membrane and specific drain design. This optimizes the rinsing of products that inhibit microbial growth.ApplicationSteritest® NEO Device for medical devices and collapsible bags is used for sterility testing of medical devices, collapsible bags and products with antimicrobial agents.Legal InformationDurapore is a registered trademark of Merck KGaA, Darmstadt, Germany
NOVASEPTUM is a registered trademark of Millipore AB - Sweden
STERITEST is a registered trademark of Merck KGaA, Darmstadt, GermanyПараметрыQuality Level 400, material Nylon 66 adapter (for needle), PVC tubing (double lumen), PVDF membrane, plain filter, stainless steel (for needle), styrene-acrylonitrile (SAN) (for canister) Agency/Method EP (2.6.1), JP (4.06), USP 71 sterility sterile; -irradiated Торговая марка Steritest® packaging pkg of 10 blisters per box, Single packed parameter 3.1 bar max. inlet pressure (45 psi) at 25 °C, 45 °C max. temp. application(s) sterility testing: suitable tubing L 850 mm color red Canister Base matrix Durapore® pore size 0.45 µm pore size input sample type pharmaceutical(s) test parameters sample volume: 120 mL (graduation marks at 25, 50, 75 and 100 mL) Featured Industry Pharmaceutical shipped in ambient Узнать цену -
Steritest® NEO Device TZHVLV205
eCl@ss: 32014001 NACRES: NB.24 General descriptionDevice Configuration: 2 canisters
Steritest® NEO is a membrane filtration device for sterility testing of filterable pharmaceutical products. The device simplifies every aspect of testing, from handling to traceability. The closed system ensures that pharmaceutical products are never exposed to the environment, minimizes false positives, and offers the highest levels of quality & reliability. This test system offers an optimized and fully regulatory compliant testing process when used with the Steritest® Symbio pump, specific accessories and high-quality culture media and rinsing fluids. The Steritest® NEO Double Packed Device for liquids in large vials is gamma sterilized and double packed for the quick transfer into sterility testing environments, simplifying decontamination procedures and saving time. A vented needle adapter vents and transfers the test product from large volume containers with a septum to the Steritest® NEO devices. The red canister base indicates low absorption. Durapore® hydrophilic Poly vinylidene fluoride (PVDF) membrane and specific drain design. This optimizes the rinsing of products that inhibit microbial growth.ApplicationSteritest® NEO Device is used for sterility testing of liquids in large vials containing antimicrobial agents.Legal InformationDurapore is a registered trademark of Merck KGaA, Darmstadt, Germany
STERITEST is a registered trademark of Merck KGaA, Darmstadt, GermanyПараметрыQuality Level 400, material Nylon 66 adapter (for needle), PVC tubing (double lumen), PVDF membrane, plain filter, stainless steel (for needle), styrene-acrylonitrile (SAN) (for canister) Agency/Method EP (2.6.1), JP (4.06), USP 71 sterility sterile; -irradiated Торговая марка Steritest® packaging pkg of 10 blisters in 2 bags of 5 blisters per box, Double packed parameter 3.1 bar max. inlet pressure (45 psi) at 25 °C, 45 °C max. temp. application(s) sterility testing: suitable tubing L 850 mm color red Canister Base matrix Durapore® pore size 0.45 µm pore size input sample type pharmaceutical(s)
liquidtest parameters sample volume: 120 mL (graduation marks at 25, 50, 75 and 100 mL) Featured Industry Pharmaceutical shipped in ambient Узнать цену -
Steritest® racks SYMBRACK2
eCl@ss: 32014001 NACRES: NB.24 General descriptionThe Steritest® rack can only be used together with the Steritest® carrying trays. The combination of 4 Steritest® carrying trays and a Steritest® rack enables the user to simultaneously and safely transport 20 media-filled canisters. The Steritest® carrying trays and Steritest® rack can remain in the incubator.ApplicationSteritest® racks are used to streamline the workflow and increase safety during laboratory filtration and sterility testing.Legal InformationSTERITEST is a registered trademark of Merck KGaA, Darmstadt, GermanyПараметрыmaterial stainless steel Agency/Method EP 2.6.1, JP 4.06, USP 71 Торговая марка Steritest® packaging pkg of (2 racks per pack) application(s) sterility testing: suitable input sample type pharmaceutical(s) Featured Industry Pharmaceutical compatibility for use with Steritest® NEO Devices, for use with Steritest® Symbio Pump, standard for VHP (Autoclavable) shipped in ambient Узнать цену -
Steritest® Symbio LFH Pump Kit, 2 media
eCl@ss: 32014001
Кат. номер SYMBLFH01BR SYMBLFH01CN SYMBLFH01DK SYMBLFH01EU SYMBLFH01IN SYMBLFH01IT SYMBLFH01 SYMBLFH01MX SYMBLFH01SZ SYMBLFH01UK SYMBLFH01AS SYMBLFH01US SYMBLFH01JP General descriptionWith its compact design, the Steritest® Symbio LFH Pump can be used comfortably in the smallest testing environments, including in the laminar flow hood, biosafety cabinet, clean room or even inside an isolator.ApplicationThe Steritest Symbio LFH Pump, designed to fit your testing environmentComponentsPeristaltic pump
Guides quality certificate
Bottle holder
Drain tray
Silicone drain tubing
Communication hub
Power cord
Network cable
USB flash drive
3 quick guidesLegal InformationSTERITEST is a registered trademark of Merck KGaA, Darmstadt, GermanyПараметрыAC/DC input 100 V / 240 V AC, 50-60 Hz material 316L stainless steel cover (for pump head), 316L stainless steel head (of pump), 316L stainless steel holder (for bottle), 316L stainless steel housing (for screen), 316L stainless steel pump, 316L stainless steel support (for drain tray), EPDM rubber seal, glass window(s) (toughened), polyester keys, polyphenylsulfone (PPSU) container (for drain tray), polyphenylsulfone (PPSU) guide(s) (for tubing), silicon seal Agency/Method EP 2.6.1, JP 4.06, USP 71 Торговая марка Steritest® application(s) sterility testing: suitable Overall H 41.0 cm (16.1 in.) , with accessories overall W 63.3 cm (24.9 in.) , with accessories overall depth 37.2 cm (14.6 in.) , with accessories pump body H 27.2 cm (10.7 in.) pump body W 33.3 cm (13.1 in.) pump body depth 37.2 cm (14.6 in.) pump head H 15.8 cm (6.2 in.) weight 14.2 kg (31.3 lb ), (pump body), 15.8 kg (34.8 lb ), (overall)with standard accessories input sample type pharmaceutical(s) Featured Industry Pharmaceutical compatibility standard for VHP Узнать цену -
Steritest® Syringe Support SYMBSYS01
eCl@ss: 32014001 NACRES: NB.24 General descriptionThe STERITEST® Syringe Support is an accessory designed to be used with the STERITEST® EZ device for prefilled syringes with needles. The Syringe support valve is connected to the STERITEST® pump through a dedicated port on the pump communication hub. The distribution of sterile fluid to dilute the contents of the syringe is controlled by an automatic valve, eliminating the necessity to turn the dilution bottle over between each syringe tested. The STERITEST® Syringe Support is compatible with all STERITEST® Equinox and STERITEST® Symbio pumps. For STERITEST® Equinox pumps, the standard bottle holder needs to be replaced by a STERITEST® Symbio complete bottle holder >(SYMBBTH01), including the removable bottle basket. This accessory is autoclavable (except for the removable automatic valve) and resistant to vaporized hydrogen peroxide (VHP) and peracetic acid decontamination cycles in isolators.ApplicationThe STERITEST® Syringe Support is an accessory used to hold the syringe, and aids in the safe handling of syringes with needles. This accessory streamlines the workflow and increases safety during laboratory filtration and sterility testing.ComponentsNALegal InformationSTERITEST is a registered trademark of Merck KGaA, Darmstadt, GermanyПараметрыmaterial 316L stainless steel , EPDM rubber (foam), Nylon 66 (glass bead reinforced), Nylon , PVC , acrylonitrile-butadiene-styrene (ABS) , anodized aluminum , brass (nickel-plated), polyoxymethylene , polyphenylsulfone (PPSU) Agency/Method EP 2.6.1, JP 4.06, USP 71 Торговая марка Steritest® application(s) sample preparation: suitable (laboratory filtration), sterility testing: suitable input sample type pharmaceutical(s) Featured Industry Pharmaceutical compatibility for use with Steritest® Symbio Pump, standard for VHP shipped in ambient Узнать цену -
Steritest® vent needles TEFG02525
eCl@ss: 32014001 NACRES: NB.24 General descriptionSteritest® vent needle is an accessory of the Steritest® NEO devices, used for liquid transfer and rinsing during sterility testing. It is a single needle vented with PTFE (hydrophobic) membrane.ApplicationThe Steritest® vent needles are used for venting glass vials with rubber septa and rigid plastic vials. They can also be used for rinsing of medical devices, vial-to-vial aseptic transfer of large volume parenteral, sterility and growth promotion qualification of media batches, or for venting of media bottles during the direct inoculation method.Legal InformationSTERITEST is a registered trademark of Merck KGaA, Darmstadt, GermanyПараметрыQuality Level 400 material PTFE (hydrophobic membrane filter), PVC device, stainless steel (for needle) Agency/Method EP (2.6.1), JP (4.06), USP 71 sterility sterile; ethylene oxide treated packaging pkg of 25 units Торговая марка Steritest® application(s) sterility testing: suitable filter size 24.7 mm pore size 0.2 µm pore size input sample type pharmaceutical(s) Featured Industry Pharmaceutical shipped in ambient Узнать цену -
Thioglycollate Broth (USP Alternative)
NACRES: NA.74
Кат. номер 70157-VAR 70157-500G 70157-100G 70157-2.5KG ApplicationA medium for sterility tests and the cultivation of microaerophilic and anaerobic organisms.Preparation NoteSuspend 29 g in 1 litre of distilled water. Bring to the boil and dissolve the medium completely. Distribute into tubes or bottles and sterilize by autoclaving at 121°C for 15 minutes. Prepare freshly or boil and cool the medium just before use!Other NotesSterility testsFootnoteWe offer two media types: the superior granulated GranuCult® and the cost-efficient powdered NutriSelect® culture media, depending on your needs.
The designations basic, plus, or prime are added to indicate the quality control level, from basic quality control to standard QC plus to prime for full regulatory compliance.Legal InformationGRANUCULT is a registered trademark of Merck KGaA, Darmstadt, Germany
NutriSelect is a registered trademark of Merck KGaA, Darmstadt, GermanyПараметрыQuality Level 200 sterility non-sterile form powder shelf life limited shelf life, expiry date on the label composition L-cystine, 0.5 g/L , dextrose, 5.5 g/L , pancreatic digest of casein, 15.0 g/L , sodium chloride, 2.5 g/L , sodium thioglycolate, 0.5 g/L , yeast extract, 5.0 g/L Торговая марка NutriSelect® Plus application(s) microbiological culture: suitable, microbiology: suitable, sterility testing: suitable final pH 7.1±0.2 (25 °C) Featured Industry Food and Beverages suitability anaerobic bacteria, nonselective for Aspergillus spp., nonselective for Bacillus spp., nonselective for Bacteroides spp., nonselective for Candida spp., nonselective for Clostridium spp., nonselective for Escherichia coli, nonselective for Pseudomonas spp., nonselective for Staphylococcus spp., nonselective for bacteria (General Media), nonselective for coliforms
Safety Informationpictograms GHS08 signalword Danger hcodes H334 pcodes P261 - P284 - P304 + P340 - P342 + P311 - P501 Personal Protective Equipment Eyeshields, Gloves, type N95 (US) RIDADR NONH for all modes of transport WGK Germany WGK 3 Flash Point F Not applicable Flash Point C Not applicable Узнать цену
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