1.46317

Tryptic Soy Broth Ready-to-use Bottles

bottle capacity 100 mL, bottle filling volume 100 mL, closure type, blue crimp cap with septum, pack of 70 bottles

• Synonim(y): CASO, Casein Soybean Digest Broth, SCDB, TSB, Tryptic Soy Broth, Tryptone Soya Broth
• NACRES: NA.74
• UNSPSC Code: 41106226
• Bottle capacity: 100 mL
• Bottle filling volume: 100 mL
• Feature: closure type blue crimp cap with septum, ready-to-use
• Agency: EP 2.6.1, JP 4.06, USP 71
• Ph: 7.1-7.5

Właściwości

• Quality Level: 300
• agency: EP 2.6.1, JP 4.06, USP 71
• sterility: sterile; autoclaved (tested for 7 days at 30-35°C)
• form: liquid
• shelf life: 360 days
• feature: closure type blue crimp cap with septum, ready-to-use
• composition: Dipotassium Hydrogen Phosphate, 2.5 g , Glucose Monohydrate, 2.5 g , Pancreatic Digest of Casein, 17 g , Papaic Digest of Soya Bean Meal, 3 g , Sodium Chloride, 5 g
• packaging: pack of 70 bottles
• bottle capacity: 100 mL
• bottle filling volume: 100 mL
• pH: 7.1-7.5
• application(s): cosmetics; food and beverages; 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

Opis

General description

Tryptic Soy Broth is a universal complex medium for the isolation and cultivation of fastidious aerobic bacteria, yeasts, and molds. It supports the growth of a wide variety of aerobic and facultative anaerobic microorganisms, including fungi by the content of two highly nutritious peptones.

Application

Tryptic Soy Broth is used for sterility testing of substances, preparations and products as well as a pre-enrichment broth for the test for specified microorganisms or total viable aerobic count determinations using the MPN method within non-sterile 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.

Other Notes

Production will take place at Millipore SAS in Molsheim, France. Deliveries will be executed in accordance with the terms and conditions of MLS RTU GmbH. A minimum order quantity is required to process the order. Once the order is placed and confirmed, Merck will ensure product delivery within a maximum timeframe of 10 to 12 weeks. The terms and conditions of Merck KGaA apply to both Millipore SAS and MLS RTU GmbH and can be accessed through the following link: Standard Terms & conditions

This medium can be modified and/or supplemented based on the required performance criteria.

Legal Information

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

Disclaimer

This item is created at the customer′s request as a customized product and will not be developed or qualified in accordance with the Merck Product Development Process.

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Informacja o środkach bezpieczeństwa

• Klasa składowania: 12 - Non Combustible Liquids
• wgk: WGK 2