LABORATOIRES URGO
FR-MF-000002559 · France · CHENOVE
LABORATOIRES URGO is registered in the European database on medical devices as a manufacturer, with 471 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIb | 319 |
|---|---|
| Class IIa | 152 |
Among these devices, 327 are declared sterile.
Devices declared under this manufacturer
- ALGOPLAQUE
- ALGOPLAQUE FILM
- SANYRENE
- URGO K2
- URGO K2 Lite
- URGO KTwo
- URGOCLEAN Pad
- URGOCRÊPE
- URGOSTART
- URGOSTART Plus Pad
- URGOSTART Tül
- URGOTUL
Showing 12 of 471 declared devices.
Catalogue references include 603551, 603783, 604370, 604672, 754163, 754167.
European nomenclature codes declared: M040499, M03040199, M04040602, M04040601, M0304010102, M03040299.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | LABORATOIRES URGO (FR) · FDA 9615662 |
| Devices in EUDAMED | 471 |
| Country of registration | France |
Device-level evidence
| Devices with a numeric GTIN | 471 |
|---|---|
| Found in the U.S. device database | 1 |
| Share | 0.2 % |
Canadian market access
| Health Canada licence listing | Licensed in Canada |
|---|---|
| Matched entry | LABORATOIRES URGO |
What it holds in Canada
| Licences on record | 11 |
|---|---|
| Currently active | 0 |
| Class 2 devices | 11 |
| First licensed | 2008-05-07 |
Licence types: Device Family (8), Single Device (3).
Licensed under: URGOCELL AG/SILVER, URGOTUL AG/SILVER, URGOTUL ABSORB, URGOTUL, URGOTUL ABSORB BORDER, URGOTUL AG/SILVER.
North American profile: Both markets. LABORATOIRES URGO is registered in both the United States and Canada.