Sanitas Healthcare Limited
IE-MF-000043566 · Ireland · Dublin
Sanitas Healthcare Limited is registered in the European database on medical devices as a manufacturer, with 5 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 5 |
|---|
Most frequent device types declared: Alcatel 1S, HY-008 Endoscope Camera, Single Use Macintosh, Size 3 Blade, Video Laryngoscope Single Use J Blade, Video laryngoscope blade – Macintosh 4.
Among these devices, 5 are declared active.
Devices declared under this manufacturer
- Protect Video Laryngoscope Blade Mac 4
- Protect Video Laryngoscope System
- Protect Video laryngoscope System
- Video Protect Video Laryngoscope J Blade
- Video Protect Video laryngoscope blade – Macintosh 3
Catalogue references include SKU SAN235PR /PRT11168, SKU SAN241PR / PRT11163, SKU SAN242PR / PRT11164, SKU SAN247PR / PRT11166, SKU SAN248PR /PRT11169.
European nomenclature codes declared: R9002, Z12021004.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 5 |
| Country of registration | Ireland |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 5 |
|---|---|
| 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. Sanitas Healthcare Limited was not found in either the U.S. or the Canadian register.