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KHVES3TTT1

Millipore

Millipore Express® SHRP, Opticap® XLT Capsule

Opticap® XLT 30, sterile, inlet connection diam. 1.5 in., pore size 0.5/0.1 μm, cartridge nominal length 30 in. (75 cm)

Sinonimo/i:

Opticap Sterile XLT 30 Millipore Express SHR with prefilter 0.5/0.1 μm 1-1/2 in. TC

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About This Item

Codice UNSPSC:
23151806

Materiali

polyester support
polyethersulfone
polypropylene (gamma-stable)
polypropylene housing
polypropylene vent cap (Gamma stable)
polysulfone
silicone seal

Livello qualitativo

Conformità normativa

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

Sterilità

irradiated
sterile

Nome Commerciale

Opticap® XLT 30

Caratteristiche

hydrophilic

Produttore/marchio commerciale

Millipore Express®

Parametri

≤91.2 mL/min air diffusion at 3.45 bar (50 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
100 psi max. differential pressure (6.9 bar) (intermittent)
2.1 bar max. differential pressure (30 psid) at 25 °C (Reverse; intermittent)
2.75 bar max. inlet pressure (40 psi) at 60 °C
25 °C max. inlet temp.
5.5 bar max. differential pressure (80 psid) at 25 °C (Forward)
5.5 bar max. inlet pressure (80 psi) at 25 °C
6.9 bar max. differential pressure (100 psid) at 25 °C (Forward; intermittent)
6.9 bar max. inlet pressure (100 psi) at 25 °C (intermittent)
80 psi max. differential pressure (5.5 bar) (continuous)
80 psig max. inlet pressure

tecniche

sterile filtration: suitable

Lunghezza

87.1 cm (34.3 in.)

Lunghezza nominale della cartuccia

30 in. (75 cm)

Diametro

19.8 cm (7.8 in.)

Superficie filtrante

1.62 m2

Diam. connessione ingresso

1.5 in.

Amp. ingresso/ uscita

15.2 cm (6.0 in.)

Diam. connessione uscita

1.5 in.

Impurezze

≤0.25 EU/mL bacterial endotoxins (LAL test, Aqueous extraction)
<0.25 EU/mL USP bacterial endotoxins (LAL test, sample aqueous extraction)

Matrice

Millipore Express® SHR (w/Prefilter)

pore size

0.5/0.1 μm pore size

Punto di bolla

≥2586 mbar (37.5 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
(38 mm (1 1/2 in.) Sanitary Flange Inlet and Outlet)

Descrizione generale

Device Configuration: Capsule
T-line/Gauge Port: T-line

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 installation section of OPTICAP® XL Capsules and OPTICAP® XLT Capsules 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 @ 123 °C; not in-line steam sterilizable
This product was manufactured with a Millipore Express® 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.
TOC/Conductivity
After sterilization and a controlled water flush of 60 L, samples exhibited less than 500 ppb TOC per USP <64> and less than 1.3 µS/cm per USP <64> at 25 °C.
Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥6 L

Note legali

ASTM is a registered trademark of American Society for Testing and Materials
MILLIPORE EXPRESS is a registered trademark of Merck KGaA, Darmstadt, Germany
OPTICAP is a registered trademark of Merck KGaA, Darmstadt, Germany

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