RAYS S.p.A.
IT-MF-000009229 · Italy · Osimo
RAYS S.p.A. is registered in the European database on medical devices as a manufacturer, with 120 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 120 |
|---|
Most frequent device types declared: Non Sterile Adhesive Plaster, Non Sterile Cut Gauze, Non Sterile Elastic Bandages, Non Sterile Examination Glove, Non Sterile Folded Cotton Gauze.
Devices declared under this manufacturer
- BIO FIX
- BIO OXYDE
- BIO PAP
- BIOSAFE PF HIGH RISK
- BIOSAFE PP TYPE 50
- BIOSOFT PF BLACK 35
- BIOSOFT PF COBALT FOOD
- Benda di Garza Idrofila Orlata
- Bende Elastiche Ideal
- COMPRESSE DI GARZA PIEGATA
- Camice da Laboratorio
- Compresse di Garza Tagliata
Showing 12 of 120 declared devices.
Catalogue references include 201020W, 504030W, DAR NI FOOD / XL, FIX09NBSP, K19X3N1NZB, N2000120ZC.
European nomenclature codes declared: M050101, T01020204, T010201, A06030301, M0304010102, M0201010102.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 120 |
| 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 | 120 |
|---|---|
| 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. RAYS S.p.A. was not found in either the U.S. or the Canadian register.