STOL - MIK BOGDAN MIKODA
PL-MF-000011510 · Poland · Zawiercie
STOL - MIK BOGDAN MIKODA is registered in the European database on medical devices as a manufacturer, with 18 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 18 |
|---|
Most frequent device types declared: STOLIK OKULISTYCZNY.
Among these devices, 18 are declared active.
Devices declared under this manufacturer
- STOLIK OKULISTYCZNY STM-1
- STOLIK OKULISTYCZNY STM-2
- STOLIK OKULISTYCZNY STM-2-1
- STOLIK OKULISTYCZNY STM-2K
- STOLIK OKULISTYCZNY STM-2KI
- STOLIK OKULISTYCZNY STM-2U
- STOLIK OKULISTYCZNY STM-2U-1
- STOLIK OKULISTYCZNY STM-3
- STOLIK OKULISTYCZNY STM-3L
- STOLIK OKULISTYCZNY STM-3L-1
- STOLIK OKULISTYCZNY STM-5
- STOLIK OKULISTYCZNY STM-5-0
Showing 12 of 18 declared devices.
Catalogue references include OPHTHALMIC TABLE STM-3L, OPHTHALMIC TABLE STM-5, OPHTHALMIC TABLE STM-5-0, STOLIK OKULISTYCZNY STM-1, STOLIK OKULISTYCZNY STM-2-1, STOLIK OKULISTYCZNY STM-2K.
European nomenclature codes declared: Z12129001.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 18 |
| 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 | 18 |
|---|---|
| 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. STOL - MIK BOGDAN MIKODA was not found in either the U.S. or the Canadian register.