LABORATORIOS HERBITAS, S.L.
ES-MF-000004599 · Spain · FOIOS, VALENCIA
LABORATORIOS HERBITAS, S.L. is registered in the European database on medical devices as a manufacturer, with 205 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 205 |
|---|
Most frequent device types declared: ORTESIS POSTQUIRURGICA PRO, SERIE MASTER 1/2 kg.
Devices declared under this manufacturer
- BLANDA BLANDA
- DUPLO
- Kaps FOOT MORNING: CORECTUS
- Kaps FOOT MORNING: DUOSAFE
- Kaps FOOT MORNING: MEDI GEL SEPARATOR
- Kaps FOOT MORNING: METATARSAL MED COVER
- Kaps FOOT MORNING: SEPARATOR
- Kaps FOOT MORNING: SINGLE TUBE
- Kaps FOOT MORNING: TOE CAP
- Kaps FOOT MORNING: TOES SEPARATOR
- PODIABLAND
- SERIE MASTER
Showing 12 of 205 declared devices.
Catalogue references include 103_2007_S / KAPS11.053.20, 11.007.1, 11.051.9, 11.053.12, 12.719.12, 12.720.33.
European nomenclature codes declared: Y061203, Y99, Y060499, Y061203,Y99.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 205 |
| Country of registration | Spain |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 205 |
|---|---|
| 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. LABORATORIOS HERBITAS, S.L. was not found in either the U.S. or the Canadian register.