MEDI-LINE S.A.
Medical devices - Medi-Line
Do not hesitate to contact us if you have needs in extrusion, injection or manufacturing of medical devices in clean rooms for the medical or pharmaceutical sector, we will evaluate your request with interest and professionalism. To contact us, you can go through our Linked-In page
- Type
- Manufacturer
- Location
- Angleur Liege, Belgium
- Website
- https://mediline.be
- Categories
- Medical & Healthcare Supplies
Listed in a source registry
Verified facts
- fda-registered (green), checked 2026-08-14 FDA
- debarment-clear (green), checked 2026-08-14 OpenSanctions
- corporate-mail-on-domain (green), checked 2026-08-14 Mail server of the company domain
- sanctions-clear (green), checked 2026-08-14 OpenSanctions
- fda-contract-manufacturer (green), checked 2026-08-14 FDA
- facility-registered (green), checked 2026-08-07 US FDA device establishment registration (openFDA)
Claimed certifications
- FDA Registered FDA Establishment Registration
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)