KTGRA02NN3

Aervent^® 0,2 µm, Opticap^® XL Cápsula

Opticap^® XL 2, inlet connection diam. 1/4 in., pore size 0.2 μm, cartridge nominal length 2 in. (5 cm)

• Sinónimos: Opticap XL 2 with Aervent - 2" 0.2um NPT/NPT 3pk
• Código UNSPSC: 23151806
• eCl@ss: 32031690

Propiedades

• Materiales: PTFE ; polypropylene ; polypropylene housing; polypropylene vent cap; silicone seal
• Nivel de calidad: 400
• esterilidad: non-sterile
• Compatibilidad de esterilización: autoclavable compatible
• Línea del producto: Opticap^® XL 2
• Características: hydrophobic
• fabricante / nombre comercial: Opticap^®
• Parámetros: 1.0 bar max. differential pressure (15 psid) at 80 °C (Forward); 1.0 bar max. inlet pressure (15 psi) at 80 °C; 2.75 bar max. inlet pressure (40 psi) at 60 °C; 25 °C max. inlet temp.; 4.1 bar max. differential pressure (60 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 25 °C; 80 psig max. inlet pressure
• técnicas: gas filtration: suitable
• Longitud: 5.6 in.
• Anchura: 3.3 in.
• longitud nominal del cartucho: 2 in. (5 cm)
• Diámetro: 8.4 cm (3.3 in.)
• filtración área: 0.1 m²
• diám. conexión a entrada: 1/4 in.
• diám. conexión a salida: 1/4 in.
• impurezas: <0.5 EU/mL USP bacterial endotoxins (LAL test, sample aqueous extraction)
• extraíbles gravimétricos: ≤15 mg
• matriz: Aervent^®
• tamaño de poro: 0.2 μm pore size
• Adaptador: 1/4 in. drain/vent hose barb (with double O-ring Seal); (6 mm (1/4 in.) NPT Inlet and Outlet)

Descripción

Descripción general

Device Configuration: Capsule

Envase

Double Easy-Open bag

Otras notas

These products are manufactured in a facility which adheres to FDA Good Manufacturing Practices.

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 Steam Sterilization & Integrity Testing Procedures guide and first page of Visual Inspection Guide
• Storage Statement: Store in dry location
• Disposal Statement: Dispose of in accordance with applicable federal, state and local regulations.

Nota de preparación

Sterilization Method
30 autoclave cycles of 30 min @ 135 °C; not in-line steam sterilizable

This product was manufactured with a PTFE membrane which meets the criteria for a "non-fiber releasing" filter as defined in 21 CFR 210.3 (b) (6).

Nota de análisis

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: after 24 hours in a 70/30% IPA/water mixture at controlled room temperature

Información legal

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

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

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

Cláusula de descargo de responsabilidad

EMD Millipore Corporation certifies that this product complies with the European Pressure Equipment Directive, 97/23/EC of 29 May 1997. This product has been classified under Article 3 § 3 of the Pressure Vessel Directive. It has been designed and manufactured in accordance with sound engineering practice to ensure safe use. In compliance with Article 3 § 3 of this Pressure Vessel Directive, this product does not bear the CE mark.