FLUID THIOGLYCOLLATE MEDIA FOR STERILITY

Code: STBMFTM12DP D2-231

Analysis Note

Turbidity indicates growth

Application

Sterility testing (membrane filtration and direct inoculation)Bioburden testing

Fluid ...


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€134.00 EACH
€164.82 inc. VAT

Analysis Note

Turbidity indicates growth

Application

Sterility testing (membrane filtration and direct inoculation)Bioburden testing

Fluid 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), Staphylococcus aureus (ATCC 6538) and Pseudomonas aeruginosa (ATCC 9027). This medium is used for sterility testing by membrane filtration or direct inoculation.

Components

Screw cap with septum

Culture Medium

Fluid Thioglycollate

General description

Fluid Thioglycollate Medium (FTM) is a critical component of our STERITEST® solution. The product has been formulated and tested to meet the requirements of the EP 2.6.1, USP 71, and JP 4.06. Our manufacturing approach ensures the highest level of quality for our media, improves accuracy and significantly reduces the risk of incorrect interpretation and false results. The sterilized double Tyvek® packaging allows to streamline the cleaning procedures, to minimize the risk of cross-contamination in laminar flow hoods and to secure an efficient decontamination of isolator chambers. The fluid appears light yellow, slightly opalescent and viscous 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 reduces the risk of cross-contamination and growth inhibition.

Legal Information

Tyvek is a registered trademark of E. I. du Pont de Nemours and Company

STERITEST is a registered trademark of Merck KGaA, Darmstadt, Germany

agencyin accordance with JP 4.06, in accordance with EP 2.6.1, in accordance with USP 71
application(s)pharmaceutical, sterility testing
bottle volume125 mL
compatibilityfor use with Steritest®
featureclosure type Screw Cap with Septum, ready-to-use
formliquid
inputsample type pharmaceutical(s)
packagingdouble packed of 12 × 100 mL
parameter100 mL filling volume
pH7.1±0.2 (25 °C)
Quality Level400
shipped inambient
sterilitysterile; ethylene oxide treated
storage temp.2-30°C
suitabilityanaerobic bacteria
This product has met the following criteria to qualify for the following awards:



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