KTGRA05FF1

Capsule Opticap^® XL, Aervent^® 0.2 µm

inlet connection diam. 3/4 in., Opticap^® XL 5, pore size 0.2 μm, cartridge nominal length 5 in. (13 cm)

• Sinonimo/i: Aervent KTGR Opticap XL5 Capsule
• Codice UNSPSC: 23151806
• eCl@ss: 32031690

Proprietà

• Materiali: PTFE ; polypropylene ; polypropylene housing; polypropylene support; polypropylene vent cap; silicone seal
• Livello qualitativo: 400
• Sterilità: non-sterile
• Compatibilità con la sterilizzazione: autoclavable compatible
• Nome Commerciale: Opticap^® XL 5
• Caratteristiche: hydrophobic
• Produttore/marchio commerciale: Aervent^®
• Parametri: ≤12 mL/min air diffusion at 965 mbar (14 psig) and 23 °C (in 70/30%IPA/water); ≤12 mL/min nitrogen diffusion at 970 mbar (14 psig) and 23 °C (in 70/30% IPA/water); 1.0 bar max. differential pressure (15 psid) at 80 °C (Forward); 1.0 bar max. inlet pressure (15 psi) at 80 °C (Forward); 2.8 bar max. inlet pressure (40 psi) at 60 °C (Forward); 25 °C max. inlet temp.; 4.1 bar max. differential pressure (60 psid) (Reverse; intermittent); 4.1 bar max. inlet pressure (60 psi) (Reverse; Intermittent); 5.5 bar max. differential pressure (80 psid) at 25 °C (Forward); 5.5 bar max. inlet pressure (80 psi) at 25 °C (Forward); 80 psig max. inlet pressure
• tecniche: gas filtration: suitable
• Lunghezza: 8.5 in.
• Larghezza: 4.2 in.
• Lunghezza nominale della cartuccia: 5 in. (13 cm)
• Diametro: 10.7 cm (4.2 in.)
• Superficie filtrante: 0.32 m²
• Diam. connessione ingresso: 3/4 in.
• Amp. ingresso/ uscita: 21.0 cm (8.3 in.)
• Diam. connessione uscita: 3/4 in.
• Impurezze: <0.25 EU/mL USP bacterial endotoxins (LAL test, aqueous extraction)
• Estraibili (gravimetria): ≤14 mg/cartridge
• Matrice: Aervent^®
• Dimensione pori: 0.2 μm pore size
• input: sample type gas
• Punto di bolla: ≥1100 mbar (16 psig), nitrogen with 70/30% IPA/water at 23 °C
• Raccordi: 1/4 in. drain/vent hose barb (with double O-ring Seal); inlet sanitary flange; outlet sanitary flange; (19 mm (3/4 in.) Sanitary Flange Inlet and Outlet)

Descrizione

Descrizione generale

Device Configuration: Capsule

Caratteristiche e vantaggi

Rated for aerosol retention of a total challenge of 108–1010 plaque forming units of ΦX-174 virus particles at 85 Nm3/h (50 SCFM) per cartridge.

Confezionamento

Double Easy-Open bag

Qualità

Retains Brevundimonas diminuta liquid aerosol for 21 days at a minimum challenge of 10⁷ CFU/cm²

Nota sulla preparazione

Sterilization Method
30 autoclave cycles of 30 min @ 135 °C

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

Risultati analitici

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

Gravimetric Extractables: after 24 hours in a 70/30% IPA/water mixture at controlled room temperature

HydroCorr: ≤0.38 mL/min @ 2.6 bar (38 psig) per sample

Altre note

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 Steam Sterilization & Integrity Testing Procedures guide and first page of Visual Inspection Guide
• Storage Statement: Store in dry location
• Disposal Statement: Dispose of in accordance with applicable federal, state and local regulations.

Note legali

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

ASTM is a registered trademark of American Society for Testing and Materials

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

Esclusione di responsabilità

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.