GIFRER BARBEZAT
FR-MF-000011164 · France · Vaulx-en-Velin
GIFRER BARBEZAT is registered in the European database on medical devices as a manufacturer, with 23 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIb | 16 |
|---|---|
| Class IIa | 7 |
Among these devices, 16 are declared sterile.
Devices declared under this manufacturer
- Isonasal
- Isonasin Septo
- Kruidvat Isotone Zoutoplossing
- Kruidvat Physiological Isonasal
- LAMIDERM
- Nez Bouché - Solution eau de mer Hypertonique
- PHYSIOLOGICA
- PHYSIOLOGICA ISONASAL
- PHYSIOLOGICA SEPTINASAL
- Physiologica
- Physiologica septinasal unidoses
- Septinasal unidoses
Showing 12 of 23 declared devices.
Catalogue references include 60000043, 60000077, 60000565, 60000578, 60000799, 60000855.
European nomenclature codes declared: M04040101,Q0299,Q030103,R060203, Q030103, M9099.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 23 |
| Country of registration | France |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 22 |
|---|---|
| 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. GIFRER BARBEZAT was not found in either the U.S. or the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
40562 | issued | 2031-06-24 |