Samarit Medical AG
CH-MF-000016280 · Switzerland · Zumikon
Samarit Medical AG is registered in the European database on medical devices as a manufacturer, with 21 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 21 |
|---|
Most frequent device types declared: Hightec, Professional, Rollbord Blue Transfer, Rollbord EcoLite, Rollbord Transglide.
Authorised representative in the Union: Samarit Medical Produkt GmbH.
Devices declared under this manufacturer
- Rollbord Blue Transfer L/N
- Rollbord Blue Transfer S/W
- Rollbord EcoLite 120
- Rollbord EcoLite 180
- Rollbord EcoLite 90
- Rollbord Hightec MRI/CT/AMBU
- Rollbord Hightec Mini-Gyn
- Rollbord Hightec ICU / Bariatric
- Rollbord Hightec Standard
- Rollbord Professional Ambulance
- Rollbord Professional MRI
- Rollbord Transglide Pull sheet
Showing 12 of 21 declared devices.
Catalogue references include 420.2002, 440.0300, 440.1090, 440.1120, 440.1180, 440.2400.
European nomenclature codes declared: V080504, V0804.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | SAMARIT MEDICAL AG (CH) · FDA 3014872186 |
| Devices in EUDAMED | 21 |
| Country of registration | Switzerland |
Device-level evidence
| Devices with a numeric GTIN | 21 |
|---|---|
| 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: United States only. Samarit Medical AG is registered in the United States but was not found in the Canadian register.