CVPB51PK1

Vitipore^® II Plus Cartridge Filter

sterile; γ-irradiated, nominal pore size 0.45 μm, cartridge nominal length 10 in. (25 cm), Code 5 (2-222; O-rings and spear)

• 동의어(들): Vitipore^® II Plus Cartridge Filter 10 in. 0.45 μm Code 5
• UNSPSC 코드: 23151806
• eCl@ss: 32031690

속성

• material: PVDF ; mixed cellulose esters (MCE) prefilter; polypropylene ; polypropylene support; silicone seal
• 규정 준수: meets EU framework regulation [1935/2004/EC] (all component materials; regarding materials and articles intended to contact food); meets FDA Indirect Food Additive requirements cited in 21 CFR 177-182 (all component materials)
• 무균: sterile; γ-irradiated
• 특징: hydrophilic
• 제조업체/상표: Vitipore^®
• 파라미터: ≤17.1 mL/min air diffusion at 1.5 bar (22 psig) and 23 °C (in water); 0.35 bar max. differential pressure (5 psid) at 109 °C (Forward); 1.7 bar max. differential pressure (25 psid) at 80 °C (Forward); 3.5 bar max. differential pressure (50 psid) at 25 °C (Reverse; intermittent); 5.5 bar max. differential pressure (80 psid) at 25 °C (Forward)
• 카트리지 공칭 길이: 10 in. (25 cm)
• 직경: 6.9 cm (2.7 in.)
• 여과 면적: 0.78 m²
• 중량 추출물: ≤51 mg/cartridge
• Matrix: Vitipore^® II Plus
• 공극 크기: 0.45 μm nominal pore size; 0.45 μm pore size
• 입력: sample type food(s); sample type liquid; sample type beverage(s); sample type bottled water; sample type wine; sample type beer
• 버블 포인트(bubble point): ≥1930 mbar (28 psig), air with water at 23 °C
• 카트리지 코드: Code 5 (2-222; O-rings and spear)

설명

일반 설명

Device Configuration: Cartridge

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 Wetting Instructions for Filter Units with Durapore^® Membrane user guide
• Storage Statement: Store in dry location
• Disposal Statement: Dispose of in accordance with applicable federal, state and local regulations.

제조 메모

Sterilization Method
100 SIP cycles of 30 min @ 109 °C; hot water sanitized 50 times for 30 min @ 80 °C maximum

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

Gravimetric Extractables: after 24 hours in water at controlled room temperature

법적 정보

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

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

안전성 정보

• Storage Class Code: 11 - Combustible Solids
• WGK: WGK 2