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TZHASV205

Millipore

Steritest® NEO Device

For liquids in small vials. Blue base canister with a vented double needle for small vials with septa. Double packed.

Synonim(y):

Blue Base Steritest® NEO device for sterility testing, Sterility testing device, membrane filtration device, membrane filtration canister, closed membrane filtration

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About This Item

Kod UNSPSC:
23151818
eCl@ss:
32014001
NACRES:
NB.24

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

agency

EP (2.6.1)
JP (4.06)
USP 71

sterylność

sterile; γ-irradiated

producent / nazwa handlowa

Steritest®

opakowanie

pkg of 10 blisters in 2 bags of 5 blisters per box, Double packed

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

sample type pharmaceutical(s)
liquid

Zastosowanie

pharmaceutical
sterility testing

Warunki transportu

ambient

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, offers the highest levels of quality & reliability, and 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 device is gamma sterilized and double packed for the quick transfer into sterility testing environments, simplifying decontamination procedures and saving time. The Steritest® NEO Double Packed device contains a small diameter double needle adapter for small vials with septum. The blue canister base indicates mixed esters of cellulose membrane. This membrane provides an optimal filtration flow rate for standard products.

Zastosowanie

Steritest® NEO Device for liquids in small vials is used for sterility testing of small volume parenterals and synthetic drugs without antimicrobial activity.

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 double packed blisters in 2 bags of 5 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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Kod klasy składowania

11 - Combustible Solids

Klasa zagrożenia wodnego (WGK)

WGK 2


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Produkty

Testowanie sterylności jest jednym z najważniejszych etapów uwalniania produktów farmaceutycznych. Zgodne z przepisami urządzenia do testowania sterylności metodą filtracji membranowej zapewniają bezpieczeństwo produktów farmaceutycznych.

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