Application Note: Testing the Seal Strength of Porous Medical Device Packages

ISO Standard 11607-1:2006 - Packaging for terminally sterilized medical devices specify test methods for materials, preformed sterile barrier systems, sterile barrier systems and packaging systems.  Essentially, seal strength and package integrity must be validated to ensure the protective packaging will uphold the product’s sterile barrier and that it has no channel leaks.

Learn how finished, porous, sterilized medical device packages can be efficiently tested for seal burst strength in compliance with ASTM F2054.

Read the full application note in the Related Resources column to the right.