SUPORTH MED SRL
RO-MF-000034720 · Romania · Miercurea Ciuc
SUPORTH MED SRL is registered in the European database on medical devices as a manufacturer, with 77 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 77 |
|---|
Devices declared under this manufacturer
- PODOFIX CARBON - 100 - 44
- PODOFIX CARBON - 101 - 39
- PODOFIX CARBON - 101 - 40
- PODOFIX CARBON - 101 - 43
- PODOFIX CARBON - 101 - 44
- PODOFIX CARBON - 102 - 35
- PODOFIX CARBON - 102 - 39
- PODOFIX CARBON - 102 - 40
- PODOFIX CARBON - 103 - 47
- PODOFIX VACUUM - 27
- PODOFIX VACUUM - 33
- PODOFIX VACUUM - 36
Showing 12 of 77 declared devices.
Catalogue references include PED 100 - 44, PED 101 - 40, PED 101 - 43, PED 102 - 35, PED 102 - 40, PED 50 - 36.
European nomenclature codes declared: Y061203.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 77 |
| Country of registration | Romania |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 77 |
|---|---|
| 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. SUPORTH MED SRL was not found in either the U.S. or the Canadian register.