1.46220

Thioglycollate Medium

box of 100 tubes, ready-to-use, tube volume 9 mL , filling volume

• Sinónimos: Fluid Thioglycollate Medium, Thioglycollate Broth, FTM
• UNSPSC Code: 41106225
• NACRES: NA.74

Propiedades

• agency: EP 2.6.1; JP 4.06; USP 71
• Quality Level: 300
• description: For the isolation and cultivation of fastidious anaerobic and aerobic microorganisms
• sterility: sterile; autoclaved
• form: liquid (ready-to-use)
• shelf life: 6 mo.
• feature: closure type screw cap with septum; ready-to-use
• packaging: box of 100 tubes; single packed of (9 ml in 17 ml tube with red cap)
• tube capacity: 17 mL
• tube volume: 9 mL , filling volume
• pH: 7.1
• application(s): pharmaceutical; sterility testing
• compatibility: for use with Steritest^® Symbio FLEX Pump Kit, 2 media (SYMBFLE01); for use with Steritest^® Symbio ISL Pump Kit, 2 media (SYMBISL01); for use with Steritest^® Symbio LFH Pump Kit (SYMBLFH01)
• storage temp.: 2-25°C
• suitability: nonselective for

Descripción

General description

Fluid Thioglycolate Medium is a universal complex medium. It is recommended for sterility testing of pharmaceutical products according to the European and US Pharmacopoeia. Thioglycolate and L-Cystine in the medium reduce the redox potential of the culture medium to create an anaerobic atmosphere. Also, mercury and other heavy metal compounds are inactivated by these agents. The content of agar further reduces a rapid diffusion of oxygen through the medium but may lead to slight turbidity in larger volumes (filled bottles). Resazurin indicates the reduction potential of the medium. An increased concentration of oxygen is indicated by a color change to pink.

Application

Fluid Thioglycolate Medium is used for the isolation and cultivation of fastidious anaerobic as well as for aerobic microorganisms. This is used for sterility control of pharmaceutical products.

Features and Benefits

Our ready to use media provide the highest level of quality and testing confidence. They have been formulated and tested to meet the pharmacopoeia requirements. Sterility testing media and rinse solutions are manufactured in an ISO 9001, environmentally controlled production center. Each lot undergoes a stringent quality control (QC) procedure, including pH, sterility and growth promotion tests. Our manufacturing approach ensures the highest level of clarity for our media and rinsing fluids, therefore improving accuracy and significantly reducing the risk of incorrect interpretation and false results.

Legal Information

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

Información de seguridad

• Storage Class: 10 - Combustible liquids
• wgk_germany: WGK 2