Production requirements for packaging sterile medical goods are extremely stringent.
As far as possible, they should be manufactured in the same environment in which they will later be used – only in so-called cleanrooms.
With their complete sterility they guarantee maximum safety.
Südpack Medica in France has state of the art ISO-certified clean rooms.
Class 100 000 or ISO 8 to ISO 14644-1 for the manufacture of bags.
Class 10 000 or ISO 7 to ISO 14644-1 for the manufacture and printing of blister lids and storage containers.
In and outside the clean room, the quality of our products is subject to ongoing and stringent controls. This also applies to the raw materials used.
| Certification ISO 13485 |
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| Certification ISO 9001 |
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