Sanicen S.A.
ES-MF-000000738 · Spain · HUECAS
Sanicen S.A. is registered in the European database on medical devices as a manufacturer, with 116 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 116 |
|---|
Devices declared under this manufacturer
- GUANTE DE NITRILO AZUL SIN POLVO DELTALAB EUROTUBO – 100 UDS – T. L
- GUANTE DE NITRILO AZUL SIN POLVO DELTALAB EUROTUBO – 100 UDS – T. M
- GUANTE DE NITRILO AZUL SIN POLVO DENTAL IBÉRICA – 100 UDS – T. XS
- GUANTE DE NITRILO NEGRO SIN POLVO SANYC SENSITIVE – 100 UDS – T. M
- GUANTE DE NITRILO SIN POLVO ECO - 100 UDS - T. XL
- GUANTE DE NITRILO SIN POLVO NEW MARK – 100 UDS – T. S
- GUANTE LATEX CON POLVO DENTALIBERICA – T.XS
- GUANTE LATEX S/P SANYC T/L TEX
- GUANTE LATEX SENSITIVE SIN POLVO SANYC S 100U
- GUANTE LÁTEX CON POLVO NEW MARK – T.L
- GUANTE LÁTEX SIN POLVO NEW MARK – T.L
- GUANTE LÁTEX SIN POLVO NEW MARK – T.M
Showing 12 of 116 declared devices.
Catalogue references include 001281T, 11003, 118411, 128111, 1410, 1411.
European nomenclature codes declared: T01020204, T010201, T01020201.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 116 |
| 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 | 116 |
|---|---|
| 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. Sanicen S.A. was not found in either the U.S. or the Canadian register.