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MOLDED PRODUCT

Medical-Grade Liquid Silicone Rubber (LSR)

Medical-grade LSR liquid silicone compounds for injection molding in an ISO 8 cleanroom. Compliance with USP VI, ISO 10993, FDA 21 CFR 177.2600, and EC 1935/2004. Biocompatibility, purity, and total traceability for medical, pharmaceutical, and laboratory applications.

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Medical-Grade Liquid Silicone Rubber (LSR)
Certification ISO 10993 · USP VI · FDA
Catalysis Platinum
Tolerance ISO 3302-1 · M2
Implantable Short term (≤29 days)

Material Principle

Medical LSR liquid silicone is a two-component, platinum-cured elastomer formulated specifically for high-purity environments. It enables the fully automated injection molding of medical, pharmaceutical, and in-vitro diagnostic components with micrometric tolerances.

Formulation and Certifications

Compliant with regulations USP Class VI, ISO 10993, FDA 21 CFR 177.2600, and EC 1935/2004. Free of byproducts, plasticizers, and heavy metals. Sterilizable by autoclave, steam, or gamma radiation. Each batch is supplied with traceability and a certificate of conformity.

Technical Properties

Available in hardnesses from 20 to 90 Shore A. High transparency, thermal stability from -60 °C to +230 °C, and excellent chemical resistance. Physiologically inert, non-cytotoxic material suitable for prolonged contact with tissues and bodily fluids.

Production Environments

Production in a validated ISO 8 cleanroom under ISO 9001 and ISO 13485 quality systems. Auditable, controlled, and traceable processes, with biocompatibility, accelerated aging, and dimensional validation tests.

Product Gallery

Technical Specifications

Key Technical Data

Typical values obtained according to series datasheets (17, 30) and indicated standards. May vary based on hardness, formulation, and application. Final validation is the customer's responsibility.

Property Typical Values Standard
Hardness (Shore A) 20 – 70 (núcleo habitual: 40–60) ISO 7619-1
Tensile Strength 7 – 11 MPa ISO 37
Elongation at Break 400 – 1200 % ISO 37
Tear Resistance (Type C) 17 – 47 kN/m ISO 34-1
Density 1,11 – 1,20 g/cm³ ISO 2781
Working Temperature –60…+200 °C (up to +215 °C in some formulations)
Tolerances Molding Class M2 (LSR Injection) ISO 3302-1
Sectoral (On Request) FDA / CE 1935/2004 / USP VI / ISO 10993 / RoHS / REACH
Guaranteed Quality

Certifications and Regulatory Compliance in Silicone Molding

Every molding batch is manufactured under strict validation protocols, guaranteeing conformity with international standards and integral traceability of the material and the mold.

Main Certifications

  • ISO 9001:2015 – Quality Management System
  • ISO 13485:2016 – Medical Devices
  • EN 9100 – Aerospace and Defense
  • GMP – Good Manufacturing Practices
  • ISO 10993 – Medical Biocompatibility
  • USP Class VI – Pharmaceutical Biocompatibility

Regulatory Compliance

  • FDA 21 CFR 177.2600 – Food Contact
  • EC 1935/2004 – Materials in Contact with Food
  • EN 45545-2 – Railway Fire Protection
  • UL94 – Material Flammability
  • ISO 10993 and USP Class VI – Medical and Pharmaceutical Biocompatibility
  • REACH (1907/2006) and RoHS (2015/863) – Chemical and Electrical Substances

Key Applications

Certified Production

Manufacturing and Delivery Options

  • Hardness: 10 to 80 Shore A
  • Colors: Translucent, pigmented, or optical grade
  • Formulation: 100% platinum cure, byproduct-free
  • Certifications: USP VI, ISO 10993, FDA, EC 1935/2004
  • Production: Certified ISO 8 Cleanroom
  • Delivery: Sterilizable, traced, and certified parts
Selection Guide

Product Selection Matrix

Customer Requirement Recommended Solution
Food-contact componentsFood-Grade LSR
High-precision technical partsHCR Injection Molding
Medical and optical microcomponentsLSR Injection Molding
Integration with inserts or multi-component systemsOvermolding
In Summary

Technical Conclusion and Recommendations

Medical LSR liquid silicone from ProSilicones64 represents the highest standard in biocompatibility, precision, and purity for the healthcare sector.

Manufactured in an ISO 8 cleanroom under ISO 9001 and ISO 13485 control, and certified according to USP VI, ISO 10993, and FDA, it ensures safety and total traceability in critical applications.

A solution designed for new-generation medical devices that demand absolute performance, cleanliness, and stability.

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