H3D
FR-MF-000009082 · France · LAVANCIA-EPERCY
H3D is registered in the European database on medical devices as a manufacturer, with 18 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 18 |
|---|
Among these devices, 2 are declared sterile.
Devices declared under this manufacturer
- Kit complet Family - Tick Twister
- Kit complet Family - Tick Twister [DE]
- Kit complet Family DE/FR - Tick Twister SUPAIR
- Kit complet Kids - Tick Twister [DE]
- Kit complet Kids Tick Twister - DE/FR
- Mosquito Zecken Haken
- Tick Twister
- Tick Twister - Blister Outdoor
- Tick Twister - Etui Clipbox
- Tick Twister - Etui Silicone
- Tick Twister - Kit complet Family NL/FR - ID PHAR
- Tick Twister - Kit complet Kids NL/FR - ID PHAR
Showing 12 of 18 declared devices.
Catalogue references include ETUICLIPBOX3C, KITFAMILYIDPHAR, KITFAMILYSUPAIR, KITPLA3TTFAMILY, KITTTFAMILYDE, KITTTKIDSDE.
European nomenclature codes declared: V901099.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 18 |
| 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 | 18 |
|---|---|
| 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. H3D was not found in either the U.S. or the Canadian register.