KGW6A02HH3

Polysep^™ II 1.0/0.5 µm nominal, Opticap^® XL Capsule

inlet connection diam. 9/16 in., Opticap^® XL 2, pore size 1.0/0.5 μm, cartridge nominal length 2 in. (5 cm)

• Szinonimák: Opticap XL2 Polysep II 1.0/0.5 μm 9/16 in. HB/HB
• UNSPSC kód: 23151806
• eCl@ss: 32031610

Tulajdonságok

• material: borosilicate glass fiber (BGF) prefilter; mixed cellulose esters (MCE) ; polypropylene ; polypropylene housing; polypropylene support; polypropylene vent cap; silicone seal
• Minőségi szint: 400
• szab. megfelelőség: meets FDA Indirect Food Additive requirements cited in 21 CFR 177-182 (all component materials)
• sterilitás: non-sterile
• Sterilizálási kompatibilitás: autoclavable compatible
• termékcsalád: Opticap^® XL 2
• Jellemzők: hydrophilic
• gyártó/kereskedő neve: Opticap^®
• parameter: 1.0 bar max. inlet pressure (15 psi) at 80 °C; 2.75 bar max. inlet pressure (40 psi) at 60 °C; 25 °C max. inlet temp.; 3.5 bar max. differential pressure (50 psid) at 25 °C; 5.5 bar max. inlet pressure (80 psi) at 23 °C; 80 psig max. inlet pressure
• technika/technikák: prefiltration: suitable
• Hosszúság: 14.2 cm (5.6 in.)
• Szélesség: 3.3 in.
• patron névleges hossza: 2 in. (5 cm)
• Átmérő: 14.5 cm (5.7 in.)
• szűrőfelület: 0.06 m²
• bemeneti csatl. átmérője: 9/16 in.
• bemenettől kimenetig Sz: 14.2 cm (5.6 in.)
• kimeneti csatl. átmérője: 9/16 in.
• szennyeződések: ≤0.5 EU/mL bacterial endotoxins (LAL test, Aqueous extraction); <0.5 EU/mL USP bacterial endotoxins (LAL test, sample aqueous extraction)
• gravimetriás extrahálható anyagok: ≤45 mg/capsule
• Mátrix: Polysep^™ II
• pore size: 1.0/0.5 μm nominal pore size; 1.0/0.5 μm pore size
• bemenet: sample type liquid
• szerelvény: inlet hose barb; outlet hose barb; (14 mm (9/16 in.) Hose Barb Inlet and Outlet)

Leírás

Általános leírás

Device Configuration: Capsule

Tulajdonságok és előnyök

Format: Double Layer

Kiszerelés

Double Easy-Open bag

Egyéb megjegyzések

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 to the first page of Visual Inspection Guide and introduction section of the Mixed cellulose esters Tech Brief
• Storage Statement: Please refer to the Mixed cellulose esters Tech Brief
• Disposal Statement: Dispose of in accordance with applicable federal, state and local regulations.

Kapcsolódás

Replaces: SN1M017A01

Elkészítési megjegyzés

Sterilization Method
3 autoclave cycles of 30 min @ 121 °C; not in-line steam sterilizable

This product was manufactured with a media combination which meets the criteria for a "non-fiber releasing" filter as defined in 21 CFR 210.3 (b) (6).

Analízis megjegyzés

Gravimetric Extractables: after a 600 mL flush and 24 hours in water at controlled room temperature

Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥1 L

Jogi információk

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

Polysep is a trademark of Sigma-Aldrich Co. LLC

Jogi nyilatkozat

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.

Biztonsági adatok

• Tárolási osztály kódja: 11 - Combustible Solids
• WGK: WGK 2