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ANSI/AAMI/ISO 11607-1:2006

Packaging for terminally sterilized medical devices - Part 1: Requirements for materials, sterile barrier systems and packaging

AAMI/ISO 11607-1 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 to the point of use.


Content Provider
Association for the Advancement of Medical Instrumentation [aami]


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Document History
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As the voice of the U.S. standards and conformity assessment system, the American National Standards Institute (ANSI) empowers its members and constituents to strengthen the U.S. marketplace position in the global economy while helping to assure the safety and health of consumers and the protection of the environment.

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