UA-44035381-1
  • AseptiFlex™ TPE Tubing

AseptiFlex™ TPE Tubing

mdi AseptiFlex™ thermoplastic elastomer (TPE) tubing offers a reliable solution for process requiring fluid transfer and management.

AseptiFlex™ tubing are manufactured in certified clean rooms and have been validated to meet standardregulatory and functional requirements for critical applications ranging from aseptic sampling to sterilefilling of drug products.

  • Heat weldable
  • Heat sealable
  • Uniform, smooth inner bore for efficient fluid flow
  • Tube welding for sterile fluid pathway connections
  • Tube sealing for sterile fluid pathway disconnections
  • Single use bag and tubing assemblies
Specifications
Hardness 60 Shore A
Operational
Sterilization By Autoclave at 125°C for 30 minutes, 1 cycle
Sterilization By Irradiation up to 50 kGy
Shelf Life MDI TPE tubing has a shelf life of 5 years.
Assurance
Bioburden Bioburden level is < 1000 cfu/device as per ISO 1737-1:2018.
Fiber Release Passes test as per USP and comply with USFDA Title 21 CFR Part 210.3(b)(6) for fiber release.
Particle Release Complies with USP <788> test for particulate matter in injections.
Indirect Food Additive These PCS tubing meet the FDA Indirect Food Additive requirements cited in 21 CFR 177.1520.
Endotoxin Testing Aqueous extracts exhibit <0.25 EU/ml as established by Limulus Amebocyte Lysate (LAL) Test as per USP <85>.
Non Animal Origin The materials used for manufacture of mdi tubing do not contain substance of animal origin as per EMEA/410/01 Rev. 03.
Extractables Extractable profiles for TPE tubing are available as per BioPhorum Best Practices Guide for Extractable Testing of Polyemric Single Use Components used in Biopharmaceutical Manufacturing.
Sterility
The gamma sterilization process for gamma sterilized tubing has been validated as per ISO 11137 to ensure a sterility assurance level (SAL) of 10-6.
Package Integrity MDI tubing with 15 M roll length are packed in double polyethylene bags to ensure package integrity during transit as well as to prevent particulate contamination.
Biosafety Passes Biological Reactivity test, In-Vivo, as per USP<88> for Class VI plastics. Passes the Biological Reactivity Tests, In Vitro for Cytotoxicity as described in USP<87>.
To order, please specify the catalog number and quantity.
Example: AFTT031063AXX01, 2 rolls
Brochure/Leaflet Download