Orphée SA
CH-MF-000050926 · Switzerland · Plan-les-Ouates
Orphée SA is registered in the European database on medical devices as a manufacturer, with 46 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
Authorised representative in the Union: PZ CORMAY Spółka Akcyjna.
Devices declared under this manufacturer
- MYT-3CRP H
- MYT-3CRP L
- MYT-3CRP N
- MYTHIC 18
- MYTHIC 3CRP CRP-L
- MYTHIC 3CRP Cleaner
- MYTHIC 3CRP Diluent
- MYTHIC 3CRP Lysing Reagent
- MYTHIC 60
- MYTHIC 70
- MYTHIC CRP Calibrators
- Myt-5D
Showing 12 of 46 declared devices.
Catalogue references include HM18-008-05, HM18-009-20, HM3CRP-002-05, HM3CRP-003-10, HM3CRP-6CAL, M70AL.
European nomenclature codes declared: W0103010105, W0103010501, W0103010502, W0103010507, W01029003, W0103010503.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 46 |
| 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 | 46 |
|---|---|
| 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. Orphée SA was not found in either the U.S. or the Canadian register.