Diaglobal GmbH
DE-MF-000032608 · Germany · Berlin
Diaglobal GmbH is registered in the European database on medical devices as a manufacturer, with 30 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
Most frequent device types declared: Diaglobal Photmeter, Diaglobal Photometeer, Diaglobal Photometer, Photometer.
Devices declared under this manufacturer
- Bilirubin
- Cholesterin
- Creatine Kinase
- Erythroctes
- Erytrocten Eckküvetten
- Glucose
- Harnstoff
- Hämatokrit
- Hämoglobin
- Hämoglobin Eck-Küvetten
- Hämoglobin Eckküvetten
- Hämoglobin Kontrolle
Showing 12 of 30 declared devices.
Catalogue references include BIL 142, CK 321, DP550, ERY 040, GLU 142, HB 040.
European nomenclature codes declared: W0103010601, W0103010602, W0103010606, W02010199, W01010113, W0103010603.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 30 |
| 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 | 2 |
|---|---|
| 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. Diaglobal GmbH was not found in either the U.S. or the Canadian register.