KHGEA2ZTH1

Cápsula Millipore Express^® SHC, Opticap^® XLT

Opticap^® XLT 20, inlet connection diam. 1.5 in., pore size 0.5/0.2 μm, cartridge nominal length 20 in. (50 cm)

• Sinônimo(s): Autoclavable Opticap XLT 20 Millipore Express SHC 0.5/0.2 μm TC/HB 1pk w/gauge port
• Código UNSPSC: 23151806

Propriedades

• Materiais: polyethersulfone ; polypropylene ; polypropylene housing; polypropylene support; polypropylene vent cap; polysulfone ; silicone seal
• 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^® XLT 20
• Características: hydrophilic
• fabricante/nome comercial: Millipore Express^®
• Parâmetros: 1.0 bar max. inlet pressure (15 psi) at 80 °C; 1000 bar max. differential pressure (15 psi) at 80 °C (Forward); 2.75 bar max. inlet pressure (40 psi) at 60 °C; 2100 bar max. differential pressure (30 psi) at 25 °C (Reverse; intermittent); 25 °C max. inlet temp.; 5.5 bar max. inlet pressure (80 psi) at 25 °C; 5500 mbar max. differential pressure (80 psi) at 25 °C (Forward); 6.9 bar max. inlet pressure (100 psi) at 25 °C (intermittent); 6900 mbar max. differential pressure (100 psi) at 25 °C (Forward; intermittent); 80 psig max. inlet pressure
• técnica(s): sterile filtration: suitable
• Comprimento: 61.1 cm (24.0 in.)
• Largura: 7.8 in.
• comprimento nominal do cartucho: 20 in. (50 cm)
• Diâmetro: 19.8 cm (7.8 in.)
• área de filtração: 0.98 m²
• diâm. conexão de entrada: 1.5 in.
• diam. conexão de saída: 5/8 in.
• Impurezas: ≤0.25 EU/mL bacterial endotoxins (LAL test, Aqueous extraction); <0.25 EU/mL USP bacterial endotoxins (LAL test, sample aqueous extraction)
• Matriz: Millipore Express^® SHC
• pore size: 0.5/0.2 μm pore size
• ponto de bolha: ≥4000 mbar (58 psig), air with water at 23 °C
• conector: 3/4 in. gauge port (T-Line Side); inlet sanitary flange; outlet hose barb; 1/4 in. vent hose barb (with double O-ring Seal); (38 mm (1 1/2 in.) Sanitary Flange Inlet and 16 mm (5?8 in.) Hose Barb Outlet)

Descrição

Descrição geral

Device Configuration: Capsule

T-line/Gauge Port: T-line with 3/4 in. Gauge Port T-line side

Embalagem

Double Easy-Open bag

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

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

This product was manufactured with a Millipore Express^® 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.

TOC/Conductivity
After sterilization and a controlled water flush of 40 L, samples exhibited less than 500 ppb TOC per USP <64> and less than 1.3 µS/cm per USP <64> at 25 °C.

Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥4 L

Informações legais

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

MILLIPORE EXPRESS 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.