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Merck

TZHVDV205

Millipore

Steritest® NEO Device

For soluble powders in vials with septa. Red base canister with vented double needle for small vials with septa. Double packed.

別名:

Red 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

UNSPSCコード:
23151818
eCl@ss:
32014001
NACRES:
NB.24

物質

Nylon 66 adapter (for needle)
PVC tubing (double lumen)
PVDF membrane
plain filter
stainless steel (for needle)
styrene-acrylonitrile (SAN) (for canister)

品質水準

認証

EP (2.6.1)
JP (4.06)
USP 71

無菌性

sterile; γ-irradiated

メーカー/製品名

Steritest®

包装

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

パラメーター

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.

チューブの長さ

850 mm

red Canister Base

マトリックス

Durapore®

ポアサイズ

0.45 μm pore size

入力

sample type pharmaceutical(s)

アプリケーション

pharmaceutical
sterility testing

輸送温度

ambient

詳細

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 ensures that pharmaceutical products are never exposed to the environment, minimizes false positives, and offers the highest levels of quality & reliability. 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 device simultaneously dissolves/dilutes the sample in sterile diluent and transfers the resulting solution to canisters. A small diameter double needle adapter is used for small vials with septum. The red canister base indicates low absorption. Durapore® hydrophilic Poly vinylidene fluoride (PVDF) membrane and specific drain design. This optimizes the rinsing of products that inhibit microbial growth.

アプリケーション

Steritest® NEO Device is used for sterility testing of antibiotics and products with antimicrobial activity that require dilution or dissolution.

特徴および利点

  • 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 fromall 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.

包装

Pack of 10 double packed blisters in 2 bags of 5 blisters per box

法的情報

Durapore is a registered 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

以下の用途に設定されています


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