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Merck
CN

KVGLA2TTT1

Millipore

Durapore® 0.22 µm, Opticap® XLT Capsule

Opticap® XLT 20, inlet connection diam. 1.5 in., cartridge nominal length 20 in. (50 cm)

Synonym(s):

Opticap XLT20 Durapore 0.22 μm 1-1/2 in. TC/TC

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About This Item

UNSPSC Code:
23151806

material

PVDF
polypropylene
polypropylene housing
polypropylene support
polypropylene vent cap
silicone seal

Quality Level

reg. compliance

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

sterility

non-sterile

Sterilization Compatibility

autoclavable compatible

product line

Opticap® XLT 20

feature

hydrophilic

manufacturer/tradename

Opticap®

parameter

≤26.6 mL/min air diffusion at 2.75 bar (40 psig) and 23 °C (in water)
1.0 bar max. inlet pressure (15 psi) at 80 °C
1.7 bar max. differential pressure (25 psid) at 80 °C (Forward)
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

technique(s)

sterile filtration: suitable

L

62.5 cm (24.6 in.)

cartridge nominal length

20 in. (50 cm)

diam.

10.7 cm (4.2 in.)

filtration area

1.4 m2

inlet connection diam.

1.5 in.

inlet to outlet W

15.2 cm (6.0 in.)

outlet connection diam.

1.5 in.

impurities

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

gravimetric extractables

≤50 mg/capsule

matrix

Durapore®

pore size

0.22 μm

input

sample type liquid

bubble point

≥3450 mbar (50 psig), air with water at 23 °C

fitting

1/4 in. drain/vent hose barb (with double O-ring Seal)
(38 mm (1 1/2 in.) Sanitary Flange Inlet and Outlet)

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General description

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

Packaging

Double Easy-Open bag

Other Notes

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.

Preparation Note

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).

Analysis Note

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 ≥2 L

Legal Information

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

Disclaimer

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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Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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  1. How frequently do the various consumables need to be changed?

    The frequency that consumables must be changed depends on the system's usage (treated water volume) and on the consumables themselves (time of usage). In order to ensure the quality of water and your results, the consumables should be replaced when the system alerts you.

  2. What is the consumables delivery time?

    Refer to the consumable's Product page for a first estimation of its expected delivery time and contact customer service for more information.

  3. How are consumables changed?

    To help you to change your system's consumables, several video tutorials are available on our YouTube channel: Milli-Q®System Care Tutorials. For high-flow systems, please keep in mind that all consumable changes must be approved by a 3-digit code that only the person in charge of the system knows.

  4. What is the shelf life for Filter?

    The shelf life is 2 years for all consumables kept in the recommended storage conditions (temperatures from 5 to 30°C; humidity between 10 and 80%). Contact your local representative for more information.

  5. Can I arrange to have my consumables automatically ordered and delivered once a year?

    It's possible to place only one consumable order per year with a specific contract called "Consumable Supply Agreement (CSA)" For further information, contact your local representative or sales contact.

  6. Where can I find data sheets, Certificates of Origin, Certificates of Analysis, and Certificates of Quality?

    Documents and certificates are available in the "Documentation" section on this page. Do not hesitate to contact us if you require further information.

  7. What steps are you taking towards improved sustainability?

    Sustainability is at the heart of our innovations. From reducing water and energy consumption, to minimizing plastic and chemical waste, our dedicated water system engineers are constantly working on new ways to reduce the ecological footprint of our products to better support the sustainability goals we’re all striving towards. For more information, we invite you to review the following brochure and infographic which highlight our efforts and achievements: link. Do not hesitate to contact your local representative for further information.

  8. How can I know which consumables can be used with my system?

    To know which consumables can be used on your system, you can see in the user manual of you system or see it on the following webpage of consumables. All the consumables for each system are indicated.

  9. If I have a final filter that I use only occasionally (e.g., Biopak®) and have another filter (e.g. Millipak®) that I most of the time, can I keep the 'occasional-use' filter for use again at a later time?

    It is not possible to re-use a filter that has been used and then removed because air intake during replacement creates an airlock and blocks water passing through the filter. If you regularly need two different filters, we recommend using two POD dispensers.

  10. Can consumables be opened and refilled?

    Unfortunately, this is not possible because of safety issues and the need to guarantee the quality of consumables and their interior purification components. Our consumables are manufactured in an ISO 9001-certified facility France in agreement with high quality standards.

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