adeor medical AG
DE-MF-000011451 · Germany · Valley
adeor medical AG is registered in the European database on medical devices as a manufacturer, with 7 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 7 |
|---|
Most frequent device types declared: Meridian Alpha Perforator Ø7/11 mm, 3.0 mm, Meridian Alpha Perforator Ø11/14 mm, 1.0 mm, Meridian Alpha Perforator Ø11/14 mm, 3.0 mm, Meridian Alpha Perforator Ø7/11 mm, 1.0 mm, Meridian Classic Perforator Ø11/14 mm, 2.0 mm.
Among these devices, 7 are declared sterile.
Devices declared under this manufacturer
- Meridian Alpha Cranial Perforator
- Meridian Classic Alpha Perforator
- Meridian Classic Cranial Perforator
Catalogue references include PER 11-14-S, PER 11-14-SP, PER 7-11-S, PER 7-11-SP, PER C6-9-S, PER C8-11-S.
European nomenclature codes declared: P091304.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | ADEOR MEDICAL AG (DE) · FDA 3007031059 |
| Devices in EUDAMED | 7 |
| Country of registration | Germany |
Device-level evidence
| Devices with a numeric GTIN | 7 |
|---|---|
| Found in the U.S. device database | 0 |
| Share | 0.0 % |
Canadian market access
| Health Canada licence listing | Not found in the Canadian register |
|---|
⚠️ Canada lists no Class I devices at all — what that excludes.
North American profile: United States only. adeor medical AG is registered in the United States but was not found in the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
MDR-0018 | issued | 2029-10-15 |