TZHVLV205

Steritest^® NEO Device

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

• Sinonimo/i: Red Base Steritest^® NEO device for sterility testing, Sterility testing device, membrane filtration device, membrane filtration canister, closed membrane filtration
• Codice UNSPSC: 23151818
• eCl@ss: 32014001
• NACRES: NB.24

Proprietà

• Materiali: Nylon 66 adapter (for needle); PVC tubing (double lumen); PVDF membrane; plain filter; stainless steel (for needle); styrene-acrylonitrile (SAN) (for canister)
• Livello qualitativo: 400
• agenzia: EP (2.6.1); JP (4.06); USP 71
• Sterilità: sterile; γ-irradiated
• Produttore/marchio commerciale: Steritest^®
• Confezionamento: pkg of 10 blisters in 2 bags of 5 blisters per box, Double packed
• Parametri: 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.
• Lung. tubo: 850 mm
• Colore: red Canister Base
• Matrice: Durapore^®
• Dimensione pori: 0.45 μm pore size
• input: liquid; sample type pharmaceutical(s)
• applicazioni: pharmaceutical; sterility testing
• Condizioni di spedizione: ambient

Descrizione

Descrizione generale

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 Steritest^® NEO Double Packed Device for liquids in large vials is gamma sterilized and double packed for the quick transfer into sterility testing environments, simplifying decontamination procedures and saving time. A vented needle adapter vents and transfers the test product from large volume containers with a septum to the Steritest^® NEO devices. 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.

Applicazioni

Steritest^® NEO Device is used for sterility testing of liquids in large vials containing antimicrobial agents.

Caratteristiche e vantaggi

• 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.

Confezionamento

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

Note legali

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

Informazioni sulla sicurezza

• Codice della classe di stoccaggio: 10-13 - German Storage Class 10 to 13