1.46396

Líquido D - Líquido de enjuague listo para usar

bottle capacity 1000 mL, bottle filling volume 1000 mL, closure type, White screw cap with septum and protector, pack of 6 bottles

• Sinónimos: Fluid D, Rinsing Solution, Washing fluid
• UNSPSC Code: 41106214
• NACRES: NA.72
• Bottle capacity: 1000 mL
• Bottle filling volume: 1000 mL
• Feature: closure type White screw cap with septum and protector, ready-to-use
• Agency: EP 2.6.1, JP 4.06, USP 71; 71
• Ph: 6.9-7.3

Propiedades

• Quality Segment: 300
• material: glass bottle
• agency: EP 2.6.1, JP 4.06, USP 71; 71
• sterility: sterile; autoclaved (tested for 14 days at 30-35°C and 20-25°C)
• form: liquid
• shelf life: 360 days
• feature: closure type White screw cap with septum and protector, ready-to-use
• composition: Peptic Digest of Animal Tissue, 1 g , Tween^® 80, 1 mL
• packaging: pack of 6 bottles
• technique(s): sterile filtration: suitable
• bottle capacity: 1000 mL
• bottle filling volume: 1000 mL
• pH: 6.9-7.3
• application(s): cosmetics; food and beverages; pharmaceutical; sterility testing
• storage temp.: 2-25°C
• suitability: nonselective for

Descripción

General description

Fluid D is a washingsolution for sterility testing of pharmaceutical samples containing lecithin oroil using the membrane filtration method. Rinse the membrane with Fluid D after filtration and provide a suitable mediumto observe microbial growth.

Application

Fluid D is suitablefor rinsing the solutions containing oil or lecithin during sterility testingby membrane filtration. It is also suitable for the removal of antimicrobialactivity of non-sterile products by membrane filtration. The fluid is alsoexcellent for rinsing sterile pathways of devices and is used for rinse methodtesting of medical devices.

Features and Benefits

• Our ready-to-use media provide the highestlevel of quality and testing confidence. They are formulated and tested to meetthe pharmacopeia requirements.
• Sterility testing media and rinse solutions aremanufactured in an ISO 9001, environmentally controlled production center. Eachlot undergoes a stringent quality control (QC) procedure, including pH,sterility, and growth promotion tests.
• Our manufacturing approach ensures the highest level of clarity forour media and rinsing fluids, thus improving accuracy, and reducing the risk ofincorrect 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

TWEEN is a registered trademark of Croda International PLC

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.

Información de seguridad

• flash_point_f: Not applicable
• flash_point_c: Not applicable
• Clase de almacenamiento: 12 - Non Combustible Liquids