Integra MicroFrance
FR-MF-000011524 · France · St Aubin Le Monial
Integra MicroFrance is registered in the European database on medical devices as a manufacturer, with 24 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 24 |
|---|
Among these devices, 12 are declared reusable.
Devices declared under this manufacturer
- Integra®
- MicroFrance®
Showing 12 of 24 declared devices.
Catalogue references include 3717001, 7718, 7766, CP391-4, CP391E, CP393-4.
European nomenclature codes declared: K020180, L149099, V0402, Z12149099, L0180, L0903.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | INTEGRA MICROFRANCE SAS (FR) · FDA 9680837 |
| Devices in EUDAMED | 24 |
| Country of registration | France |
Device-level evidence
| Devices with a numeric GTIN | 24 |
|---|---|
| Found in the U.S. device database | 21 |
| Share | 87.5 % |
Canadian market access
| Health Canada licence listing | Licensed in Canada |
|---|---|
| Matched entry | INTEGRA MICROFRANCE SAS |
What it holds in Canada
| Licences on record | 32 |
|---|---|
| Currently active | 0 |
| Class 2 devices | 32 |
| First licensed | 1999-10-28 |
Licence types: Device Family (21), Single Device (5), System (4), Device Group Family (2).
Licensed under: MICROFRANCE LAPROSCOPIC COAGULATION SCISSORS, MICROFRANCE ENT COAGULATION SUCTION TUBES, MICROFRANCE ENT COAGULATION PROBES, MICROFRANCE ENT COAGULATION HOOKS, MICROFRANCE SYRINGE AND INJECTION NEEDLES, MICROFRANCE ENT COAGULATION FORCEPS.
North American profile: Both markets. Integra MicroFrance is registered in both the United States and Canada.