BB/T 0059-2012 Medical device blister packaging used for co-extruded film
This part specifies the product classification, requirements, test methods, inspection rules, marking, packaging, transportation, and storage of co-extruded films for medical device blister packaging (hereinafter referred to as packaging films). This part applies to films made from polypropylene (PP), polyamide (PA), and polyethylene (PE) as raw materials, which are formed by co-extrusion processes with different structures. This part does not apply to implantable medical devices for human use.