KVGBA04TH3

Cápsula hidrofóbica Durapore^® 0,22 µm, Opticap^® XL

Opticap^® XL 4, pore size 0.22 μm

• Sinônimo(s): Durapore^® Capsule Filter 4 in. 0.22 µm
• Código UNSPSC: 23151806
• eCl@ss: 32031690

Propriedades

• Materiais: PVDF
• Nível de qualidade: 400
• conformidade reg.: meets FDA Indirect Food Additive requirements cited in 21 CFR 177-182 (all component materials)
• esterilidade: non-sterile
• Compatibilidade de esterilização: autoclavable compatible
• linha de produto: Opticap^® XL 4
• Características: hydrophobic
• fabricante/nome comercial: Durapore^®
• Parâmetros: 25 °C max. inlet temp.; 80 psig max. inlet pressure
• técnica(s): sterile filtration: suitable
• diâm. conexão de entrada: 1.5 in.
• diam. conexão de saída: 9/16 in.
• tamanho: 4 in.
• Impurezas: <0.5 EU/mL USP bacterial endotoxins (LAL test, sample aqueous extraction)
• matriz: Durapore^®
• tamanho de poro: 0.22 μm pore size
• conector: (38 mm (1 1/2 in.) Sanitary Flange Inlet and 14 mm (9/16 in.) Hose Barb Outlet)

Descrição

Descrição geral

Device Configuration: Capsule

Outras 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 installation section of OPTICAP^® XL Capsules and OPTICAP^® XLT Capsules user guide
• Storage Statement: Store in dry location
• Disposal Statement: Dispose of in accordance with applicable federal, state and local regulations.

Nota de preparo

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

Nota de análise

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

Informações legais

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

Exoneração de responsabilidade

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.