Chimed s.r.l.
IT-MF-000016095 · Italy · Livorno
Chimed s.r.l. is registered in the European database on medical devices as a manufacturer, with 57 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 57 |
|---|
Most frequent device types declared: Set per toracentesi / paracentesi, Tubo di collegamento per aspirazione chirurgica intraoperatoria.
Among these devices, 51 are declared sterile.
Devices declared under this manufacturer
- Sacca non sterile raccolta urina
- Set per toracentesi / paracentesi
- Tubo di collegamento per aspirazione chirurgica intraoperatoria
Showing 12 of 57 declared devices.
Catalogue references include 102140, MS/220/400, MS/220/500, MS/221/350, MS/301/15, MS/303/16.
European nomenclature codes declared: A060204, A060102, A06030301.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 57 |
| 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 | 57 |
|---|---|
| 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. Chimed s.r.l. was not found in either the U.S. or the Canadian register.