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-007/A-01 , LABMER-004/F-01, LABMER-002/D-01, LABMER-010/A-01, LABMER-001/D-02.
Among these devices, 10 are declared sterile, 1 active.
No authorised representative is recorded for these devices. For a manufacturer established outside the Union that would be unusual; for one established inside it, it is normal.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 60 |
| Country of registration | France |
⚠️ Absence here is not proof of absence from the market. A manufacturer may reach the United States through a distributor registered under its own name, or under a corporate name we could not match. We publish what we measured, not what we inferred.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
40111 | supplemented | 2027-10-24 |