PROTEC X-ray Systems GmbH
DE-MF-000048351 · Germany · Oberstenfeld
PROTEC X-ray Systems GmbH is registered in the European database on medical devices as a manufacturer, with 360 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 229 |
|---|---|
| Class IIb | 131 |
Among these devices, 360 are declared active, 1 with a measuring function.
Devices declared under this manufacturer
- Bucky
- Bucky WR
- CONAXX 2
- Grid entity
- Grid entity WR
- PROGNOST E
- PROGNOST SH
- PROGNOST XPE
- PROGNOST XPE-Akku
- PROVERT
- PRS 500 B
- PRS 500 C
Showing 12 of 360 declared devices.
Catalogue references include 7014-9-0000_V034, 7014-9-0000_V167, 7014-9-0000_V203, 7051-0-0170, 7051-0-3175, 7051-0-3525.
European nomenclature codes declared: Z11030599, Z11039005, Z11030503, Z11030501, Z11070701, Z11030580.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 360 |
| 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 | 360 |
|---|---|
| Found in the U.S. device database | 20 |
| Share | 5.6 % |
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. PROTEC X-ray Systems GmbH was not found in either the U.S. or the Canadian register.