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TZHALA205 Millipore

Steritest NEO devices for liquids in ampoules and collapsible bags mixed cellulose ester membrane 0,45µm 10/pk, double packed

The Steritest™ NEO Double Packed Device for liquids in ampoules or collapsible bags is used for sterility testing of large Volume Parenterals and synthetic drugs without antimicrobial activity.

  •  eCl@ss 32014001

  •  NACRES NB.24

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Properties

Related Categories Filter membranes for microbiological analysis, Filtration, Labware, Manufacturer Browser, Membrane Filters,
material   Nylon 66 adapter (for needle)
  PVC tubing (double lumen)
  blue filter
  mixed cellulose esters (MCE)
  plain filter
  stainless steel adapter (for needle)
  styrene-acrylonitrile (SAN)
sterility   sterile; γ-irradiated
mfr. no.   Steritest
parameter   3.1 bar max. inlet pressure (45 psi) at 25 °C
  45 °C max. temp.
application(s)   sterility testing: suitable
filter size   47 mm
tubing L   850 mm
matrix   MF-Millipore®
pore size   0.45 μm pore size
input   sample type pharmaceutical(s)
test parameters   sample volume: 120 mL (graduation marks at 50, 75 and 100 mL)
Agency/Method   USP 71
Featured Industry   Pharmaceutical
shipped in   ambient

Description

General description

The Steritest NEO Double Packed Device for liquids in ampoules or collapsible bags is gamma sterilized and double packed for the quick transfer into sterility testing environments, simplifying decontamination procedures and saving time. A single needle adapter enables an easy access to ampoules or collapsible bags. The blue canister base indicates mixed esters of cellulose membrane. This membrane provides an optimal filtration flow rate for standard products.

Packaging

10 ea in 2 bags of 5 blisters per box

Legal Information

MF-Millipore is a registered trademark of Merck KGaA, Darmstadt, Germany

Safety & Documentation

Safety Information

Safety Information for this product is unavailable at this time.
Protocols & Articles

Articles

Membrane Filtration Sterility Test

The membrane filtration sterility test is the regulatory method of choice for filterable pharmaceutical products, as cited in the USP <71>, EU Pharmacopoeia < 2.6.1> and JP Pharmacopoeia <4.06>.
Keywords: Absorption, Aerobic, Anaerobic, Antibiotics, Antimicrobials, Culture media, Eliminations, Filtration, Microbiology, Pharmaceutical, Sample preparations, Solvents, Veterinary

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