MAXIS a.s.
CZ-MF-000000989 · Czechia · Praha 2
MAXIS a.s. is registered in the European database on medical devices as a manufacturer, with 10 925 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 10 925 |
|---|
Devices declared under this manufacturer
- I.,PROMAX,AG,3+K protIskluz.lem,černá
- I.,S,PROMAX,AD,1K,tělová
- I.-AC rukavice,vel.1K tělová
- I.S MICRO,AD,vel.7K,lem,světlá
- I.S MICRO,AG,vel.5K,tmavá
- I.S MICRO,AG-HB LEVÁ,vel.2K,šedá
- I.S MICRO,AT,vel.6K,bronz
- II. MICRO,AG,vel.8N,krajka,bronz
- II. MICRO,AG-HB PRAVÁ,vel.7K,černá
- II.S MICRO,ATH,vel.1N,tmavá
- II.S-COMFORT COTTON,AD,vel.2+K,bílá
- II.S-COMFORT COTTON,AG,lem vel. 3K, světlá
Showing 12 of 10 925 declared devices.
Catalogue references include 8591285067250, 8591285149864, 8591285237080, 8591285279523, 8591285280253, 8591285571160.
European nomenclature codes declared: M030405, M030499.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 10 925 |
| Country of registration | Czechia |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 10 925 |
|---|---|
| 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. MAXIS a.s. was not found in either the U.S. or the Canadian register.