TZHAPC210
Steritest® NEO Device
For liquids in plastic containers. Blue base canister with a non-coring single needle minimizes blockage when piercing plastic containers.
material
Nylon 66 adapter (for needle)
PVC tubing (double lumen)
mixed cellulose esters (MCE) membrane
plain filter
stainless steel (for needle)
styrene-acrylonitrile (SAN) (for canister)
Quality Level
Agency
EP (2.6.1)
JP (4.06)
USP 71
sterility
sterile; γ-irradiated
packaging
pkg of 1 kit
manufacturer/tradename
Steritest®
parameter
120 mL sample volume (graduation marks at 25, 50, 75 and 100 mL)
3.1 bar max. inlet pressure (45 psi) at 25 °C
45 °C max. temp.
tubing L
850 mm
color
blue Canister Base
matrix
MF-Millipore™
pore size
0.45 μm pore size
input
liquid
sample type pharmaceutical(s)
application(s)
pharmaceutical
sterility testing
shipped in
ambient
Related Categories
General description
Steritest® NEO is a membrane filtration device for sterility testing of filterable pharmaceutical products. The device simplifies every aspect of testing, from handling to traceability. The closed system minimizes false positives and offers the highest levels of quality and reliability. This device ensures that pharmaceutical products are never exposed to the environment during the testing process. This test system offers an optimized and fully regulatory compliant testing process when used with the Steritest® Symbio pump, specific accessories and high-quality culture media and rinsing fluids. The non-coring needle adapter with aperture on side of needle adapter minimizes the blockage. A separate vent needle is included for the transfer of the test product, culture media or rinsing buffer. The canisters with blue base indicate mixed cellulose ester (MCE) membrane, which provides an optimal filtration flow rate for standard products.
Application
Features and Benefits
- One-stop-shop for sterility testing with our devices, pumps, media, fluids, and services
- Steritest® devices are manufactured in our Center of Excellence in Molsheim, France, with high-quality control standards maintaining the Certificate of Quality for each lot.
- New needle design
- Smarter workflow
- Completely closed set up
- Consistent performance
- New tubing disconnection tool
Packaging
Legal Information
configured for
related product
required but not provided
Storage Class Code
11 - Combustible Solids
WGK
WGK 2
Certificates of Analysis (COA)
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705578-5MG-PW
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Articles
Sterility testing is one of the most crucial steps in pharmaceutical product release. Regulatory-compliant membrane filtration sterility testing devices ensure the safety of pharmaceutical products.
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
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