Albert Hohlkörper GmbH & Co. KG
DE-MF-000005482 · Germany · Hemer
Albert Hohlkörper GmbH & Co. KG is registered in the European database on medical devices as a manufacturer, with 115 devices declared. It has a similarly named entry in the FDA register that we have not verified.
What this manufacturer declares
| Class IIa | 115 |
|---|
Devices declared under this manufacturer
- 1oz
- Easy Wash
- Intim Wash
- Irrigator-Set
- O 3
- OtoAir
- Pharmex
- Poire à oreilles 41ml
- R-med
- Russka
- Safety
- Sanity
Showing 12 of 115 declared devices.
Catalogue references include 4109.0.10700, 5113.2.00467, 8109.2.00890, 8111.2.10000, 8504.2.00000, 8516.2.00000.
European nomenclature codes declared: G020102, Q03040299, U0899, G020102,Q03040299, A02010299, Q030199.
United States market access
| FDA establishment register | Similar name found — unverified |
|---|---|
| Matched entry | ALBERT HOHLKOERPER GMBH & CO. KG (DE) · FDA 8010730 |
| Devices in EUDAMED | 115 |
| Country of registration | Germany |
⚠️ A similar name exists; we do not assert it is the same company — why.
Device-level evidence
| Devices with a numeric GTIN | 115 |
|---|---|
| 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.