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Key Documents

KVVLA02FF3

Millipore

Capsule Opticap® XL, membrana Durapore® da 0,1 µm,

Opticap® XL 2, inlet connection diam. 3/4 in., cartridge nominal length 2 in. (5 cm)

Sinonimo/i:

Opticap XL2 Durapore 0.1 μm 3/4 in. TC/TC

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About This Item

Codice UNSPSC:
23151806

Materiali

PVDF
polypropylene
polypropylene housing
polypropylene support
polypropylene vent cap
silicone seal

Livello qualitativo

Conformità normativa

meets FDA Indirect Food Additive requirements cited in 21 CFR 177-182 (all component materials)

Sterilità

non-sterile

Compatibilità con la sterilizzazione

autoclavable compatible

Nome Commerciale

Opticap® XL 2

Caratteristiche

hydrophilic

Produttore/marchio commerciale

Opticap®

Parametri

≤3.5 mL/min air diffusion at 3.9 bar (56 psig) and 23 °C (in water)
1.0 bar max. differential pressure (15 psid) at 80 °C (Forward)
1.0 bar max. inlet pressure (15 psi) at 80 °C
2.8 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 (Reverse; intermittent)
5.5 bar max. differential pressure (80 psid) at 25 °C (Forward)
5.5 bar max. inlet pressure (80 psi) at 23 °C
80 psig max. inlet pressure

tecniche

sterile filtration: suitable

Lunghezza

13.5 cm (5.3 in.)

Lunghezza nominale della cartuccia

2 in. (5 cm)

Diametro

14.5 cm (5.7 in.)

Superficie filtrante

0.09 m2

Diam. connessione ingresso

3/4 in.

Amp. ingresso/ uscita

13.5 cm (5.3 in.)

Diam. connessione uscita

3/4 in.

Impurezze

≤0.5 EU/mL bacterial endotoxins (LAL test, Aqueous extraction)
<0.5 EU/mL USP bacterial endotoxins (LAL test, sample aqueous extraction)

Estraibili (gravimetria)

≤10 mg/capsule

Matrice

Durapore®

Dimensione pori

0.1 μm nominal pore size

input

sample type liquid

Punto di bolla

≥4830 mbar (70 psig), air with water at 23 °C

Raccordi

1/4 in. drain/vent hose barb (with double O-ring Seal)
(19 mm (3/4 in.) Sanitary Flange Inlet and Outlet)

Descrizione generale

Device Configuration: Capsule

Confezionamento

Double Easy-Open bag

Altre note

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.

Nota sulla preparazione

Sterilization Method
3 autoclave cycles of 60 min @ 126 °C; not in-line steam sterilizable
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).

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 water at controlled room temperature
Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥500 mL

Note legali

ASTM is a registered trademark of American Society for Testing and Materials
Durapore is a registered trademark of Merck KGaA, Darmstadt, Germany
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.

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