Heinemann HNO Medizintechnik GmbH
DE-MF-000046391 · Germany · Kaltenkirchen
Heinemann HNO Medizintechnik GmbH is registered in the European database on medical devices as a manufacturer, with 50 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 50 |
|---|
Most frequent device types declared: Duo.
Among these devices, 11 are declared active.
Devices declared under this manufacturer
- Compressed air handle
- Compressed air handle (new)
- ENT treatment unit MODULA M
- Ear rinsing bowl
- Instrument module MODULA-HANSEAT L
- Metal nasal olive for suction hose, M
- Nebulizer Cannula detachable
- Nebulizer for liquid complete with bottle
- Nebulizer with detachable front part and bottle
- Politzer olive L
- Politzer olive L (MODUL A-M, Modula-L)
- Politzer olive M
Showing 12 of 50 declared devices.
Catalogue references include 0120-50200, 0120-50220, 0130-50500 / 12-3104, 0140-21302, 0140-60108, 13-2200.
European nomenclature codes declared: Q0399.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 50 |
| Country of registration | Germany |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 50 |
|---|---|
| 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: Neither register. Heinemann HNO Medizintechnik GmbH was not found in either the U.S. or the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
20596GB448250930 | issued | 2030-03-31 |