KVVLA2THH1

Durapore^® 0,1 µm, Capsule Opticap^® XLT

Opticap^® XLT 20, cartridge nominal length 20 in. (50 cm), filter diam. 4.2 in. (10.7 cm)

• Code UNSPSC : 23151806

Propriétés

• Matériaux: polypropylene filter; polypropylene housing; polypropylene support; silicone seal
• Niveau de qualité: 400
• Conformité réglementaire: FDA 21CFR177-182 (all component materials)
• Stérilité: non-sterile
• Mode de stérilisation compatible: autoclavable compatible
• Gamme de produits: Opticap^® XLT 20
• Caractéristiques: hydrophilic
• Fabricant/nom de marque: Opticap^®
• Paramètres: ≤40 mL/min air diffusion at 3.9 bar (56 psig) and 23 °C (in water); 1 bar max. inlet pressure (15 psi) at 80 °C; 1.7 bar max. differential pressure (25 psid) at 80 °C (Forward:); 2.8 bar max. inlet pressure (40 psi) at 60 °C; 25 °C max. inlet temp.; 3.5 bar max. differential pressure (50 psid) at 25 °C (Reverse; intermittent); 5.5 bar max. differential pressure (80 psid) at 25 °C (Forward:); 5.5 bar max. inlet pressure (80 psi) at 23 °C; 80 psig max. inlet pressure
• Technique(s): sterile filtration: suitable
• Largeur: 7.8 in.
• Longueur nominale des cartouches: 20 in. (50 cm)
• device L: 62.5 cm (24.6 in.)
• device size: 20 in.
• Diam. du filtre: 4.2 in. (10.7 cm)
• Surface de filtration: 1.4 m²
• Diam. du raccord d'entrée: 5/8 in.
• inlet to outlet width: 19.8 cm (7.8 in.)
• Diam. du raccord de sortie: 5/8 in.
• Impuretés: ≤0.5 EU/mL bacterial endotoxins (LAL test, aqueous extraction); <0.5 EU/mL bacterial endotoxins (LAL test, sample aqueous extraction)
• Matrice: Durapore^®
• Dimension de pores: 0.1 μm pore size
• Point de bulle: ≥4830 mbar (70 psig), air with water at 23 °C
• Raccords: 16 mm (5/8 in.) fitting (hose barb inlet/oulet); 1/4 in. fitting (vent/drain hose barb with double O-ring seal); (16 mm (5?8 in.) Hose Barb Inlet and Outlet)

Description

Description générale

Device Configuration: Capsule

Conditionnement

Double Easy-Open bag

Notes préparatoires

Sterilization Method:
3 autoclave cycles of 60min at 126°C; not in-line steam sterilizable

This product was manufactured with a Durapore^® membrane which meets the criteria for a "non-fiber releasing" filter as defined in 21CFR210.3(b)(6).

Remarque sur l'analyse

Bacterial Retention: Samples were quantitatively retentive of a minimum Brevundimonas diminuta challenge concentration of 1 x 10⁷ CFU/cm² using ASTM^® F838 methodology.

Gravimetric Extractables: ≤ 50 mg per capsule after 24 hours in water at controlled room temperature.

Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥ 2 L

Autres remarques

Directions for Use:

• Organism Retention: Microorganism
• Mode of Action: Filtration (size exclusion)
• Application: BioProcessing
• Intended Use: Reduction or removal of microorganism/bioburden
• Instructions for Use: Please refer Wetting Instructions for Filter Units with Durapore^® Membrane user guide
• Storage Statement: Store in dry location
• Disposal Statement: Dispose of in accordance with applicable federal, state and local regulations

Informations légales

ASTM is a registered trademark of American Society for Testing and Materials

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

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