Inter.med
FR-MF-000000461 · France · Saint-Jean-de-la-Neuville
Inter.med is registered in the European database on medical devices as a manufacturer, with 44 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 44 |
|---|
Most frequent device types declared: C34_, C355.
Devices declared under this manufacturer
- ASPIROBAT®
- ASPIROTUB®
- BATO-NEZ
- BICARÔMES
- GRAT'LANG
- GRATTE-LANGUE
- OPENJO
Showing 12 of 44 declared devices.
Catalogue references include C102P, C106, C502, CLAN01, CLAN02, CV200S.
European nomenclature codes declared: Y0999, Q019003.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | INTER-MED, INC. (US) · FDA 2133714 |
| Devices in EUDAMED | 44 |
| Country of registration | France |
Device-level evidence
| Devices with a numeric GTIN | 44 |
|---|---|
| Found in the U.S. device database | 0 |
| Share | 0.0 % |
Canadian market access
| Health Canada licence listing | Licensed in Canada |
|---|---|
| Matched entry | INTER-MED, INC. |
What it holds in Canada
| Licences on record | 39 |
|---|---|
| Currently active | 0 |
| Class 2 devices | 28 |
| Class 3 devices | 11 |
| First licensed | 2005-08-26 |
Licence types: Device Family (17), Device Group Family (10), System (5), Device Group (4).
Licensed under: SIMPLICITY, INTERFACE (CERAMIC/ENAMEL/DENTIN PRIMER), ASPIRATORS, ASPIRATING SYRINGE, SUCTION VALVES, AIR WATER SYRINGE.
North American profile: Both markets. Inter.med is registered in both the United States and Canada.