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추천 제품
material
polyethersulfone
Quality Level
제품 라인
EMPROVE® Filter
파라미터
60 psig max. inlet pressure
장치 크기
1.3 in.
불순물
<0.25 EU/mL USP bacterial endotoxins (LAL test, sample aqueous extraction)
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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 Modus 1.3 offers a filtration area of 0.22 m2 and has a primary use in pilot/small-volume processing.
Viresolve Pro Modus Devices are typically used for filtration of pilot to mid-scale batch volumes of proteins. The Viresolve® Pro Shield 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).
분석 메모
TOC/Conductivity
After a controlled water flush of 100 L/m², samples exhibited less than 500 ppb TOC per USP <64> and less than 1.3 µS/cm per USP <64>.
After a controlled water flush of 100 L/m², samples exhibited less than 500 ppb TOC per USP <64> and less than 1.3 µS/cm per USP <64>.
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.
Emprove® 프로그램이란?
Emprove® 프로그램은 자사의 필터 그리고 일회용 구성품, 제약용 원료 물질 및 시작 물질의 종합적이고 빈틈없는 문건을 제공하는 체계입니다.
Material Qualification Dossier
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Quality Management Dossier (Open Access)
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Operational Excellence Dossier
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활성 필터
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