Fluids and Culture Media for Sterility Testing of Pharmaceutical Products

Leverantör: LIOFILCHEM S.R.L.

452080 610053 610050 442080 6100535 495030 452060 24124 459503 400210 495150 495170 400210S 400110 453010 459504 495040 495190 495200 453070 400170 495160 26124 24241 21241 24242 495020 453020 400020 493000 453060 463100 470300 452500 402500 453280 463090 400030 400230 432080 452080S 452100 453030 455208 470370 492000 495010
LIOF452080EA 510 SEK
LIOF452080 LIOF610053 LIOF610050 LIOF442080 LIOF6100535 495030. 452060. 24124. 459503. 400210. 495150. 495170. 400210S 400110. 453010. 459504. 495040. 495190. 495200. 453070. 400170. 495160. 26124. 24241. 21241-VWR LIOF24242 495020. 453020. 400020. 493000. 453060. 463100. 470300. 452500. 402500. 453280. LIOF463090 LIOF400030 LIOF400230 LIOF432080 LIOF452080S LIOF452100 LIOF453030 LIOF455208 LIOF470370 LIOF492000 LIOF495010
Fluids and Culture Media for Sterility Testing of Pharmaceutical Products
Media Beredda mikrobiologiska media

Culture media, diluting and rinsing sterile solutions for sterility testing of pharmaceutical products by membrane filtration.


  • Store at 10 to 25 °C away from light
  • Shelf life: 2 years
  • Packaging, formulation and quality control suitable for media fill trial in pharmaceutical industries
  • Some products are available with double or triple irradiated wrapping


Fluid A is a washing solution for rinsing membranes during sterility testing.


Fluid D is a washing solution recommended for dissolving oils or materials containing lecithin or a preservative and can be used for devices labeled as 'sterile pathway'.


Fluid K is a sterile diluent used for rinsing membranes during sterility and is recommended for use with substances containing petrolatum/oil.


Fluid thioglycollate medium and Tryptic soy broth are general purpose liquid enrichment culture media used for sterility control of pharmaceutical products and for cultivation and isolation of fastidious anaerobic and aerobic microorganisms.


TSB is also available as triple-wrapped and gamma-irradiated bottles, particularly suitable for use in restricted areas and for aseptic process simulations (media fill trial) in the pharmaceutical industry.


Certifikat: The composition is in accordance with the requirements of the Harmonised method in the United States (USP), European (EP) and Japanese (JP) Pharmacopoeias. Thioglycollate Medium is also in compliance with ISO 7937 for isolation of Clostridium perfringens.

Order Now

Learn more

About VWR

Avantor is a vertically integrated, global supplier of discovery-to-delivery solutions for...

Läs mer About VWR