HeVaTech GmbH
DE-MF-000023884 · Germany · Grafenberg
HeVaTech GmbH is registered in the European database on medical devices as a manufacturer, with 24 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 24 |
|---|
Most frequent device types declared: BlueCup Pro.
Among these devices, 24 are declared active.
Devices declared under this manufacturer
- 4-er Matte
- BlueCup Pro SET
- Fingergeelnkschröpfkopf
- Gelenkschröpfkopf 10cm
- Lymphmatte
- Nackenmatte
- Schröpfglas 2,5cm
- Schröpfglas 3,5cm
- Schröpfkopf Kunststoff 2,5cm
- Schröpfkopf Kunststoff 3,5cm
- Schröpfkopf Kunststoff 6cm
- Spezialglas 0,7cm
Showing 12 of 24 declared devices.
Catalogue references include 20102, 20104, 40101, 40102, 40202, 40303.
European nomenclature codes declared: Z120616.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 24 |
| 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 | 24 |
|---|---|
| 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. HeVaTech GmbH was not found in either the U.S. or the Canadian register.