ERKA Kallmeyer Medizintechnik GmbH & Co. Kommanditgesellschaft
DE-MF-000009663 · Germany · Bad Tölz
ERKA Kallmeyer Medizintechnik GmbH & Co. Kommanditgesellschaft is registered in the European database on medical devices as a manufacturer, with 344 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 344 |
|---|
Most frequent device types declared: Erkameter 125 Pro, Finesse, Finesse Child, Kobold, Kobold Selbstmesser (Kobitest).
Among these devices, 147 are declared with a measuring function.
Devices declared under this manufacturer
- Erka. Erkameter 125 Pro
- Erka. Erkaphon
- Erka. Erkaphon Duo Child
- Erka. Erkatest
- Erka. Finesse
- Erka. Finesse Child
- Erka. Finesse Light
- Erka. GREEN CUFF SUPERB
- Erka. Kobitest
- Erka. Kobold
- Erka. Perfekt
- Erka. Switch Selbstmesser
Showing 12 of 344 declared devices.
Catalogue references include 025.26492.7770, 025.28482.7770, 203.27482.7290, 219.44893.7290, 224.28493.7290, 225.20493.7290.
European nomenclature codes declared: C9005, C9006, Z1203020302.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 344 |
| 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 | 344 |
|---|---|
| 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. ERKA Kallmeyer Medizintechnik GmbH & Co. Kommanditgesellschaft was not found in either the U.S. or the Canadian register.