Dupont Liveo Pharma Advanced Pump Silicone Tubing

Liveo™ Pharma Advanced Pump Tubing

Silicone Tubing and Assemblies (Si)

CHARACTERISTICS

• Delivery form: Parts, Shapes, Tubing
• Special characteristics: Translucent, Low emissions
• Medical applications: USP-VI, ISO10993, European Pharmacopeia
• Food contact: FDA 21 CFR

PRODUCT DESCRIPTION

Translucent pharmaceutical-grade silicone tubing designed for pumping of ultrapure liquids in pharmaceutical and biotechnological manufacturing processes.
Made from biomedical-grade, tear-resistant, platinum-cured elastomer.

APPLICATIONS

For use in peristaltic pumps where durability is required.
DuPont Advanced Pump Tubing offers up to four times the pump life of standard platinum-cured silicone tubing.

FEATURES & BENEFITS

• Up to four times the pump life of standard platinum-cured silicone tubing
• Excellent flexibility and superior resiliency
• Low extractables
• Contains no organic plasticizers, phthalates, or latex additives
• No peroxide by-products, chlorophenyls, or PCBs
• Easily sterilized
• Non-wetting (hydrophobic) surface
• Made from BioMedical Grade elastomer exceeding USP® Class VI Plastics Test requirements
• Meets European Pharmacopoeia monograph 3.1.9 “Silicone elastomer for closures and tubing”
• Manufactured to FDA 21 CFR 210/211 cGMP principles
• Produced in FDA registered (CFN 1816403) and inspected healthcare facility
• High purity quality (USP 788, USP 85, ISO 11737-1)
• FDA 21 CFR 177.2600 and USP 661 Physico-chemical tests - Plastics
• Reduced material usage and process shutdowns due to extended pump life
• Reduces risk of contaminating ultra-pure liquids
• Complete traceability and consistent performance
• Rigorous change control
• Outstanding filling accuracy

COMMON TUBING PRODUCT SIZES AND BURST PROPERTIES

Note: Burst pressure values are typical and not intended for specification writing. Test method based on ASTM D380-14.
*Predicted burst pressure values were calculated using a regression formula for sizes not tested for burst strength.

QUALITY INFORMATION

The FDA registered and ISO 9001:2015 certified Healthcare Industries Materials Site (HIMS site) ensures consistent product quality.

REGULATORY AND BIOCOMPATIBILITY INFORMATION

Product regulatory documentation and health data summary are available from the DuPont website or upon request.

PACKAGING

Standard package: 15-meter coil, double-bagged in sealed polyethylene bags within a cardboard box.
Various dimensions available, including those shown in the table above.

REGULATORY

Chemical Equivalency Certificate

MECHANICAL PROPERTIES

[1]: die D

ADDITIONAL INFORMATION

Refer to “Chemical Resistance Guide For Elastomers IV” (Compass Publications, La Jolla, California) for reference.
Evaluation under actual use conditions is recommended.

LIMITATIONS

This product is not approved for hospital or patient care use, including any in vivo procedures or implantation.
Not suitable for human implantation or reproductive, obstetrical, or gynecological applications.
Users are responsible for determining safety and regulatory compliance for specific uses.
DuPont makes no representation regarding suitability for medical or pharmaceutical applications.
Under no circumstances should these materials be considered for implantation exceeding 30 days.

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