Durapore® 0.22 µm, Opticap® XL Capsule
Opticap® XL 2, inlet connection diam. 1.5 in., pore size 0.22 μm, cartridge nominal length 2 in. (5 cm)
Manufacturer: Millipore
Synonym(S): Opticap XL2 Durapore 0.22 μm 1-1/2 in. TC-9/16 in. HB
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| 3 EA | KVGLA02TH3-3-EA | In Stock | ₹ 45,403.44 |
KVGLA02TH3 - 3 EA
In Stock
Quantity
1
Base Price: ₹ 45,403.44
GST (18%): ₹ 8,172.619
Total Price: ₹ 53,576.059
material
PVDF polypropylene polypropylene housingpolypropylene supportpolypropylene vent capsilicone seal
Quality Level
400
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® XL 2
feature
hydrophilic
manufacturer/tradename
Opticap®
parameter
1.0 bar max. differential pressure (15 psid) at 80 °C (Forward)1.0 bar max. inlet pressure (15 psi) at 80 °C2.8 bar max. inlet pressure (40 psi) at 60 °C25 °C max. inlet temp.3.4 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 °C80 psig max. inlet pressure
technique(s)
sterile filtration: suitable
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Description
- General description: Device Configuration: Capsule
- Packaging: Double Easy-Open bag
- Other Notes: These products are manufactured in a facility which adheres to FDA Good Manufacturing Practices.
- Preparation Note: Sterilization Method3 autoclave cycles of 60 min @ 126 °C; not in-line steam sterilizable
- Analysis Note: Bacterial RetentionSamples were quantitatively retentive of a minimum Brevundimonas diminuta challenge concentration of 1 x 10⁷ CFU/cm² using ASTM® F838 methodology.
- Legal Information: ASTM is a registered trademark of American Society for Testing and Materials
- 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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material: PVDF polypropylene polypropylene housingpolypropylene supportpolypropylene vent capsilicone seal
Quality Level: 400
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® XL 2
feature: hydrophilic
manufacturer/tradename: Opticap®
parameter: 1.0 bar max. differential pressure (15 psid) at 80 °C (Forward)1.0 bar max. inlet pressure (15 psi) at 80 °C2.8 bar max. inlet pressure (40 psi) at 60 °C25 °C max. inlet temp.3.4 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 °C80 psig max. inlet pressure
technique(s): sterile filtration: suitable
material: __
Quality Level: __
reg. compliance: __
sterility: __
Sterilization Compatibility: __
product line: __
feature: __
manufacturer/tradename: __
parameter: __
technique(s): __
material: __
Quality Level: __
reg. compliance: __
sterility: __
Sterilization Compatibility: __
product line: __
feature: __
manufacturer/tradename: __
parameter: __
technique(s): __