Kamedi GmbH
DE-MF-000006270 · Germany · Karlsruhe
Kamedi GmbH is registered in the European database on medical devices as a manufacturer, with 23 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 23 |
|---|
Among these devices, 23 are declared active.
Devices declared under this manufacturer
- EntertainME Insektenstichheiler by heat it Lightning
- heat it App for iPhone
- heat it X QoQa
- heat it classic Dongle Lightning
- heat it classic Lightning
- heat it classic Lightning (BG)
- heat it classic Lightning (SL)
- heat it classic USB-C (BG)
- heat it classic USB-C (CZ+SK)
- heat it classic USB-C (DE)
- heat it classic USB-C (Nordics)
- heat it pro Dongle USB-C
Showing 12 of 23 declared devices.
Catalogue references include 007_00614-0, 007_00615-1, 010_00575-1, 010_00575-15, 010_00575-24, 010_00575-34.
European nomenclature codes declared: V9099.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | Kamedi GmbH (DE) · FDA 3023143124 |
| Devices in EUDAMED | 23 |
| Country of registration | Germany |
Device-level evidence
| Devices with a numeric GTIN | 23 |
|---|---|
| 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. Kamedi GmbH is registered in the United States but was not found in the Canadian register.