VPPH103NB1

Viresolve^® Pro Shield H

Virus prefilter, Viresolve^® Pro Shield H, Modus 1.3 format, filtration area 0.22 m²

• 동의어(들): Viresolve^® Pro Shield H Modus 1.3
• UNSPSC 코드: 23151806
• eCl@ss: 32031690

속성

• material: PVDF housing; polyethersulfone membrane; silicone O-ring; white device
• Quality Level: 400
• 제품 라인: EMPROVE^® Filter
• 제조업체/상표: Viresolve^®
• 파라미터: 4.1 bar max. inlet pressure (60 psig)
• 높이: 13.56 cm (5.34 in.)
• 길이 × 너비 × 높이: 13.6 cm (5.3 in.) × 18.2 cm (7.3 in.) × 9.2 cm (3.6 in.)
• 길이: 18.62 cm (7.33 in.)
• 너비: 9.22 cm (3.63 in.)
• 여과 면적: 0.22 m²
• membrane nominal area: 0.22 m²
• 중량: 1.39 kg (3.06 lb)
• 불순물: <0.25 EU/mL USP bacterial endotoxins (LAL test, sample aqueous extraction)
• 피팅: 3/4 in. inlet/outlet sanitary fitting(s); 1/8 in. integrated vent hose barb (with double O-ring seal)

설명

일반 설명

The Viresolve^® Pro Solution provides a comprehensive, flexible template solution for viral clearance within mAb and recombinant protein bioproduction. This proven viral clearance solution delivers the highest levels of retention assurance and productivity across a broad range of feed stream characteristics.

Viresolve Pro Modus Devices are typically used for filtration of pilot to mid-scale batch volumes of proteins. The Viresolve^® Pro Shield H Modus 1.3 offers a filtration area of 0.22 m² and has a primary use in pilot/small-volume processing.

특징 및 장점

• Pilot and mid scale manufacturing
• Three different size formats
• Fully self contained (hardware holder not required)
• Fully disposable single-use fluid path
• Devices 100% tested with air/water diffusion and Binary Gas Test
• Shield / Shield H 100% aerosol tested

기타 정보

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

제조 메모

This product was manufactured with materials that meet the criteria for a "non-fiber releasing" filter as defined in 21 CFR 210.3 (b) (6).

저장 및 안정성

4°C - 30°C

법적 정보

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

VIRESOLVE 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.