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ISo 11607:2006 Compliant

At TEQ, we are dedicated to assuring our customers the highest quality production of their packaging.

 According to the International Organization for Standardization (ISO), ISO 11607:  

ISO 11607-1:2006 specifies the requirements and test methods for materials, preformed sterile barrier systems, sterile barrier systems and packaging systems that are intended to maintain sterility of terminally sterilized medical devices until the point of use.

ISO 11607-1:2006 is applicable to industry, to health care facilities, and wherever medical devices are placed in sterile barrier systems and sterilized.

You can learn more about ISO 11607 and what it consists of here. 

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Have a complex thermoforming challenge? Find out how we can help with:
  • Cost-savings
  • Sustainability solutions
  • On-site clean room management
  • Lean supply chain management
  • ISO 11607 compliance
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