Laboratoire de la Mer
FR-MF-000009050 · France · Saint-Malo
Laboratoire de la Mer is registered in the European database on medical devices as a manufacturer, with 60 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 60 |
|---|
Most frequent device types declared: LABMER-001/A-15, LABMER-001/B-01, LABMER-001/D-02, LABMER-002/D-01, LABMER-002/G-08.
Among these devices, 10 are declared sterile, 1 active.
Devices declared under this manufacturer
- Biover
- Faringodol
- LIBENAR
- Libenar
- NEO SINEFRINA
- PHYSIOMER
- PHYTOSUN AROMS
- Physiomer
- Phytosun Aroms
- ProRhinel
- Prorhinel
- RESPIMER
Showing 12 of 60 declared devices.
Catalogue references include OH1301020, OH1319020, OH1913020, OH1929020, OH20130020, OH2126000.
European nomenclature codes declared: Q030199, Q030103, Q0399.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 60 |
| 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 | 60 |
|---|---|
| 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. Laboratoire de la Mer was not found in either the U.S. or the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
40111 | supplemented | 2027-10-24 |