We all know that dealing with post-market medical device returns can be complicated. They’re fragile, hazardous, and present the potential for exposure.
Off-the-shelf or non-compliant packaging presents many challenges--poor fit, form, and function; lack of protection for product fragility and sharps, and inadequate instructions--in addition to the potential risks by not using UN3373 Packaging.
Handling the return of post-market medical devices requires serious solutions.
Fortunately, Inmark understands these unique challenges and offers EU MDR regulation-compliant packaging engineered to meet your needs.
