Sudpack Medica
SÜDPACK: مفاهيم الأفلام الطبية والصيدلانية والتشخيصية
تعمل شركة SÜDPACK Medica منذ أكثر من 50 عامًا على تطوير أفلام عالية الأداء لصناعات الرعاية الصحية. أقصى معايير النظافة والجودة: جودة cGMP، غرفة نظيفة، ...
- Type
- brand seeking distribution
- Location
- Germany
- Founded
- 1989
- Website
- https://suedpack-medica.com
- Categories
- تصنيع الأدوية, اللوازم الطبية والرعاية الصحية
Verified facts
- domain-registered (green), checked 2026-08-02 Domain registry record
- vat-valid (green), checked 2026-08-01 VIES (European Commission)
- sanctions-clear (green), checked 2026-08-16 OpenSanctions
- debarment-clear (green), checked 2026-08-16 OpenSanctions
Profiles
Import rules for these goods
- Medical devices sold in the EU must carry CE marking under the Medical Device Regulation (EU) 2017/745, with a conformity assessment matched to the device risk class. European Commission (MDR)
- For the US market, the maker must have an FDA device establishment registration and product listing; most instruments also need 510(k) premarket clearance. US FDA (devices)
- Medicines imported into the EU must come from a site holding an EU GMP certificate, and the importer needs a manufacturing/import authorisation. European Medicines Agency (GMP)