Rossmax Swiss GmbH
CH-MF-000011245 · Switzerland · Heerbrugg
Rossmax Swiss GmbH is registered in the European database on medical devices as a manufacturer, with 68 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 68 |
|---|
Most frequent device types declared: AC1000f, MA350f, MW701f, NB500, NB60.
Among these devices, 38 are declared active, 21 with a measuring function.
Authorised representative in the Union: CMC Medical Devices & Drugs SL.
Devices declared under this manufacturer
- Alternating Pressure Mattress
- Cuff
- Mesh nebulizer
- Multifunction Piston nebulizer
- Piston nebulizer
- Probe cover
- Spacer for Aerosol
- Stethoscope
- Suction unit
- Temple thermometer (non-contact) (professional)
- Upper arm blood pressure monitor
- Upper arm blood pressure monitor with PARR function
Showing 12 of 68 declared devices.
Catalogue references include EB100, EB600, MA350f, MW701f, NB500, NB60.
European nomenclature codes declared: Z1203020302, R060101, V030180, C9005, R03010302, V0301010202.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 68 |
| Country of registration | Switzerland |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 32 |
|---|---|
| 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. Rossmax Swiss GmbH was not found in either the U.S. or the Canadian register.