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  • Autoclave Venting
  • Nitrogen blanketening in sterile API
  • Sterile filtration of API and injectables
  • Sterile compressed air for pharma machinery & tools
  • Vent filtration in Bioreactors ( inlet/outlet )
  • Venting of fermentors and storage tanks
  • Sterile airing for dry powder injectables filling
  • Absolute retention
  • 100% integrity tested
  • Easy identification & traceability
  • High heat stability
  • Wide chemical comptability

Materials of Construction

Membrane: Polytetrafluoroethylene
Housing: Polypropylene
Core: Polypropylene
End Connections: Polypropylene
Rings: Silicone (Only with 1/4" MNPT)

Operational Parameters

Max Temp: 80 °C @ ≤ 2 Kg/cm²
Max Pressure: 3.5 Kg/cm² @ 25 °C for forward, 0.7 Kg/cm² @ 25 °C for reverse
Autoclavable: 100 autoclave cycles @125°C, 90 autoclave cycles @135°C

Bubble Point

0.22µm: ≥ 1380 mbar (20 psi) (with 70% IPA)
0.45µm: ≥ 690 mbar (10 psi) (with 70% IPA)

Max Air Diffusion Flow (for 10″ Cartridge)

0.22µm: ≤ 40 mL/min @ 1104 mbar (16 psi) (with 70% IPA)
0.45µm: ≤ 40 mL/min @ 552 mbar (8 psi) (with 70% IPA)

Microbial Retention

0.22µm: LRV > 7 for Brevundimonas Diminuta
0.45µm: LRV > 7 for Serratia marcescens

Regulatory Compliance

Endotoxin releasing: <0.25 EU/mL as determined by the LAL test
Particle release: Meets the requirements of WFI set by USP
Non-fiber releasing: Meets the criteria for a non-fiber releasing filter as per USP
Material toxicity: All components meet the requirements of the USP Reactivity Test for Class VI Plastics Filters meet the requirements of USP Biological Reactivity Tests in Vitro Cytotoxicity
Bacterial challenge test: Filters with the claim passed the bacterial challenge testing using Brevundimonas diminuta (ATCC 19146) at a minimum challenge concentration 1x10⁷ CFU/cm² (0.22 µm) per ASTM F838-20.
Extractables: Tested according to BioPhorum Operations Group (BPOG) guideline. Report is available upon request.
Indirect food additive: Meets the FDA Indirect Food Additive requirements cited in 21 CFR 177.1520
Food contact material: (EU) No. 1935/2004, (EU) No. 10/2011
Quality: Manufactured in accordance with ISO 9001 and ISO 13485 certified quality management system
PTFE Cartridge Filter CFTF_Nupore_Flow rates

Drug Specific Filter Validation Services

Through, nSure Validation Services, we offer a complete range of filter validation services to qualify your molecules with our Filters in accordance with the requirements listed in PDA TR#26 and in compliance with international regulatory bodies such as USFDA and EU GMP.

Filter Integrity Test
Bacterial Retention Testing (BRT)
Chemical Compatibility Test
Throughput Study
Extractables & Leachables
Learn More
Laboratory Testing
Clean Room Testing
Equipment Testing