TZHAPC210

Steritest^® NEO Device

For liquids in plastic containers. Blue base canister with a non-coring single needle minimizes blockage when piercing plastic containers.

• Synonim(y): Blue Base Steritest^® NEO device for sterility testing, Sterility testing device, membrane filtration device, membrane filtration canister, closed membrane filtration
• Kod UNSPSC: 23151818
• eCl@ss: 32014001
• NACRES: NB.24

Właściwości

• Materiały: 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)
• Poziom jakości: 400
• agency: EP (2.6.1); JP (4.06); USP 71
• sterylność: sterile; γ-irradiated
• opakowanie: pkg of 1 kit
• producent / nazwa handlowa: Steritest^®
• Parametry: 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.
• dł. rurki: 850 mm
• kolor: blue Canister Base
• macierz: MF-Millipore^™
• wielkość porów: 0.45 μm pore size
• moc wejściowa: liquid; sample type pharmaceutical(s)
• Zastosowanie: pharmaceutical; sterility testing
• Warunki transportu: ambient

Opis

Opis ogólny

Device Configuration: 2 canisters

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.

Zastosowanie

The Steritest^® NEO Device is used for sterility testing of liquids in plastic containers, without antimicrobial agents.

Cechy i korzyści

• 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

The design of this new needle has been optimized with short needle length, grips, and ridges to offer dexterity and security to the operator while piercing the small container

• Smarter workflow

The new Steritest^® NEO cartridge device benefits from all the improvements such as colored clamps, graduations for accurate volume measurement, optimized identification, and traceability with the new peel-off label

• Completely closed set up

Pharmaceutical products are never exposed to the environment during the testing process with Steritest^® NEO devices. Filtration, rinsing, media addition and incubation are conducted within a closed system.

• Consistent performance

100% integrity testing, strict physical and microbiological tests performed at every step of the assembly of the Steritest^® NEO device before release from manufacturing

• New tubing disconnection tool

The Velax^® cutting clamps are mounted on all Steritest^® NEO devices and allow safe and easy cutting of the tubes.

Opakowanie

Pack of 10 single packed blisters per box

Informacje prawne

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

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

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

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Informacja o środkach bezpieczeństwa

• Kod klasy składowania: 11 - Combustible Solids
• Klasa zagrożenia wodnego (WGK): WGK 2