INMED Spółka Akcyjna
PL-MF-000009272 · Poland · Krępice
INMED Spółka Akcyjna is registered in the European database on medical devices as a manufacturer, with 91 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 5 |
|---|---|
| Class IIb | 86 |
Among these devices, 91 are declared active.
Devices declared under this manufacturer
- Jednostka zaopatrzenia medycznego - Kolumna sufitowa LISSAclassic-lift
- Jednostka zaopatrzenia medycznego - Panel nadłóżkowy MERYart
- Koncentrator tlenu 93 - seria in.OXY
- PPB-A8 Punkt poboru sprężonego powietrza do napędu narzędzi chirurgicz
- PPB-OP Punkt poboru mieszaniny gazów (O2/N2O) – typ BS
- PPB-V Punkt poboru próżni (VAC) – typ BS
- PPD-N Punkt poboru podtlenku azotu (N2O) – typ DIN
- Rury do gazów medycznych – seria in.PIPE
- Sygnalizator stanu gazów medycznych SSGM-H
- System rurociagowy do gazów medycznych i próżni - SRGM-IIa
- Wtyk kątowy AGA do próżni (VAC)
- Wtyk prosty AGA do podtlenku azotu (N2O)
Showing 12 of 91 declared devices.
Catalogue references include LISSAclassic-lift, PPB-OP, PPB-V, PPD-N, SRGM-IIa, WPA-N.
European nomenclature codes declared: Z120309.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 91 |
| Country of registration | Poland |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 91 |
|---|---|
| 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. INMED Spółka Akcyjna was not found in either the U.S. or the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
TNP/MDR/0038/4999/2025 | issued | 2028-08-06 |