Enclara Medical s.r.l.
IT-MF-000013110 · Italy · MILANO
Enclara Medical s.r.l. is registered in the European database on medical devices as a manufacturer, with 25 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 25 |
|---|
Most frequent device types declared: APF 001, BD 001, BRM 001, BRM 002, CRM 001.
Among these devices, 1 are declared active.
Devices declared under this manufacturer
- APF 001 - Asta porta flebo amagnetica MR Safe
- Barella Amagnetica MR Safe Schienale Regolabile
- Barella doccia elettrica
- Barella doccia idraulica
- CRM 001 22C - Carrello risonanza magnetica 2+2 cassetti
- CRM 001 3C3R - Carrello risonanza magnetica 3 cassetti 3 Ripiani
- CRM 001 3R - Carrello risonanza magnetica 3 ripiani
- CRM 001 4C - Carrello risonanza magnetica 4 cassetti
- CRM 001 6C - Carrello risonanza magnetica 6 cassetti
- Pannello di Lavaggio e Sanificazione
- Predellino amagnetico 2 Gradini
- SEP 001 - 205 kg Electric Mobile Lift
Showing 12 of 25 declared devices.
Catalogue references include BDI 001, CRM 001 4C, CRM 001 6C, SA1G, SA2G, SDM 001 ABA.
European nomenclature codes declared: Z1105018099, Z11059099, Y091203, Y093399, Y093312, V0805030102.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 25 |
| 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 | 25 |
|---|---|
| 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. Enclara Medical s.r.l. was not found in either the U.S. or the Canadian register.