Destlo Karol Cymerman
PL-MF-000050397 · Poland · Wtelno
Destlo Karol Cymerman is registered in the European database on medical devices as a manufacturer, with 97 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 97 |
|---|
Devices declared under this manufacturer
- Destlo 250
- Karolina Łukasik 10
- Karolina Łukasik 100
- Kodano 10
- Kodano czarny na czarną butelkę 30
- Kostulski 100
- Mia Vita
- Oko i Ucho 10
- Okular Room
- Optyk Karman
- POLO OPTIC
- Płyn czyszczący
Showing 12 of 97 declared devices.
Catalogue references include 040, 041, 044, 060, 068, 082.
European nomenclature codes declared: Z12029015.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 97 |
| 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 | 97 |
|---|---|
| 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. Destlo Karol Cymerman was not found in either the U.S. or the Canadian register.