SAPI MED S.p.A.
IT-MF-000023733 · Italy · Alessandria
SAPI MED S.p.A. is registered in the European database on medical devices as a manufacturer, with 210 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 210 |
|---|
Most frequent device types declared: BLUSCOPE MIDI SELF-LED-LIGHT, Blu-Scope, Blu-Scope Midi, LEM, Lem 4-Ring.
Among these devices, 86 are declared sterile, 11 active.
Devices declared under this manufacturer
- Adaptor
- BLUSCOPE MIDI SELF-LIGHT
- Blu-Scope
- FLASH LIGHT
- LEM
- LIGHT GUIDE
- Lem 4-Ring
- MPR Short - Multi Purpose Short Rectoscope
- Proctoscope
- Rectoscope
- SCLEROJET
- Self-Led-Light
Showing 12 of 210 declared devices.
Catalogue references include A.4021.1ST, A.4022.1ST, A.4023.1LST, A.4519LI, A.4520I, A.4520LRINS.
European nomenclature codes declared: G02060301, G020401, G06, Z129004, G02060399, A06010103.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | SAPI MED S.P.A (IT) · FDA 3004443374 |
| Devices in EUDAMED | 210 |
| Country of registration | Italy |
Device-level evidence
| Devices with a numeric GTIN | 188 |
|---|---|
| Found in the U.S. device database | 35 |
| Share | 18.6 % |
Canadian market access
| Health Canada licence listing | Licensed in Canada |
|---|---|
| Matched entry | SAPI MED S.P.A. |
North American profile: Both markets. SAPI MED S.p.A. is registered in both the United States and Canada.