WEINMANN Emergency Medical Technology GmbH
DE-MF-000005691 · Germany · Hamburg
WEINMANN Emergency Medical Technology GmbH is registered in the European database on medical devices as a manufacturer, with 8 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIb | 5 |
|---|---|
| Class IIa | 3 |
Most frequent device types declared: MEDUMAT Standard², OXYWAY Click oxygen administrator.
Among these devices, 5 are declared active, 5 with a measuring function.
Devices declared under this manufacturer
- MEDUVENT Standard
- OXYWAY Click
- OXYWAY Click+
Catalogue references include WM 28710-01, WM 28710-02, WM 28710-03, WM 28710-04, WM 31030-1, WM 31060-1.
European nomenclature codes declared: Z12030104, R0580.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | WEINMANN EMERGENCY MEDICAL TECHNOLOGY GMBH (DE) · FDA 3017365972 |
| Devices in EUDAMED | 8 |
| Country of registration | Germany |
Device-level evidence
| Devices with a numeric GTIN | 8 |
|---|---|
| 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. WEINMANN Emergency Medical Technology GmbH is registered in the United States but was not found in the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
HZ 2714059-1 | amended | 2028-05-14 |