TZHVSV205

Steritest^® NEO Device

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

• Synonym(s): Red Base Steritest^® NEO device for sterility testing, Sterility testing device, membrane filtration device, membrane filtration canister, closed membrane filtration
• UNSPSC Code: 23151818

Properties

• material: Nylon 66 adapter (for needle); PVC tubing (double lumen); PVDF membrane; plain filter; stainless steel (for needle); styrene-acrylonitrile (SAN) (for canister)
• Quality Level: 400
• Agency: EP (2.6.1); JP (4.06); USP (71)
• sterility: sterile; γ-irradiated
• manufacturer/tradename: Steritest^®
• packaging: pkg of 10 blisters in 2 bags of 5 blisters per box, Double packed
• parameter: 120 mL sample volume (graduation marks at 25, 50, 75 and 100 mL)
• color: red Canister Base
• pore size: 0.45 μm pore size
• input: liquid; pharmaceutical(s)
• application(s): pharmaceutical; sterility testing
• shipped in: ambient

Description

General description

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 Steritest^® NEO Double Packed Device for liquids in small vials is gamma sterilized and double packed for the quick transfer into sterility testing environments, simplifying decontamination procedures and saving time. The device contains a small diameter double needle adapter 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.

Application

Steritest^® NEO Device for liquids in small vials is used for sterility testing of small volume parenterals of products with antimicrobial activity.

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

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.

Packaging

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

Legal Information

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