Bericah S.p.A.
IT-MF-000007397 · Italy · Arcugnano
Bericah S.p.A. is registered in the European database on medical devices as a manufacturer, with 204 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 204 |
|---|
Most frequent device types declared: ABBIGLIAMENTO MONOUSO IN TNT NON STERILE, BENDA COESIVA, BENDA ELASTICA, CEROTTI EFFETTO FREDDO, DISPOSITIVO CON TECNOLOGIA FIR.
Devices declared under this manufacturer
- BENDA ELASTICA FREDDA
- CAMICE NON STERILE AD ALTA PROTEZIONE BIOLOGICA
- DERMA NYTRIL SP
- DERMA STRETCH
- DERMA STRETCH PLUS
- FASCIA ELASTICA PER CAVIGLIA
- MANICOTTO TNT+PE
- PROTIX
- Quadrante Igiene, guanti monouso in nitrile
- SENSI SYNTHETIC LATEX
- SENSICHLOR
- SENSILATEX
Showing 12 of 204 declared devices.
Catalogue references include 18024151806471, 39921, 42579, 70098V, BENELAFR1DP, GU115LQUIG.
European nomenclature codes declared: T01020204, T01020201, T010201, T0399, T020402, M9001.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 204 |
| Country of registration | Italy |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 204 |
|---|---|
| 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. Bericah S.p.A. was not found in either the U.S. or the Canadian register.