KVGBA04TH3

Hydrophobic Durapore^® 0.22 µm, Opticap^® XL Capsule

Opticap^® XL 4, pore size 0.22 μm

• 동의어(들): Durapore^® Capsule Filter 4 in. 0.22 µm
• UNSPSC 코드: 23151806
• eCl@ss: 32031690

속성

• material: PVDF
• Quality Level: 400
• 규정 준수: meets FDA Indirect Food Additive requirements cited in 21 CFR 177-182 (all component materials)
• 무균: non-sterile
• 멸균 적합성: autoclavable compatible
• 제품 라인: Opticap^® XL 4
• 특징: hydrophobic
• 제조업체/상표: Durapore^®
• 파라미터: 25 °C max. inlet temp.; 80 psig max. inlet pressure
• 기술: sterile filtration: suitable
• 입구 연결 직경: 1.5 in.
• 출구 연결 직경: 9/16 in.
• 크기: 4 in.
• 불순물: <0.5 EU/mL USP bacterial endotoxins (LAL test, sample aqueous extraction)
• 기질: Durapore^®
• 공극 크기: 0.22 μm pore size
• 피팅: (38 mm (1 1/2 in.) Sanitary Flange Inlet and 14 mm (9/16 in.) Hose Barb Outlet)

설명

일반 설명

Device Configuration: Capsule

기타 정보

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.

제조 메모

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).

분석 메모

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

법적 정보

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

면책조항

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.