Sudpack Medica
SÜDPACK: Tıp, Farmasötik ve Diagnostik Film Konseptleri
SÜDPACK Medica, 50 yılı aşkın süredir sağlık sektörü için yüksek performanslı filmler geliştirmektedir. Maksimum hijyen ve kalite standartları: cGMP kalitesi, temiz oda, ...
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Germany
- Founded
- 1989
- Website
- https://suedpack-medica.com
- Categories
- İlaç Üretimi, Tıbbi ve Sağlık Malzemeleri
What is established and what is not
No facet of this company has been investigated yet. The facts below are collected records, not an assessment: nothing here confirms manufacturing, ownership or trading status beyond what each record literally says.
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)