SORIMEX sp. z o.o.
PL-MF-000020958 · Poland · TORUŃ
SORIMEX sp. z o.o. is registered in the European database on medical devices as a manufacturer, with 1 229 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 1 229 |
|---|
Most frequent device types declared: EK-1, EK-S, EK-T, ZSU.
Devices declared under this manufacturer
- Adapter kabla EKG, przedłużacz kabla
- ECG Electrodes
- Elektrody EKG
- Elektrody do defibrylacji
- Kabel EKG do badań holterowskich
- Kabel SPO2
- NIBP cuff
- Zestaw Serwet Uniwersalny
- adapter NIBP
- kabel EKG do diagnostyki
- kabel EKG do monitorowania
- mankiet NIBP
Showing 12 of 1 229 declared devices.
Catalogue references include EKK-1, KB-3/0-M/0-Wb/L-60/270-32, KB-3/i-Hb/4,7-Rp/L-60/200-32, KB-5/0-4/1-76a/L-90/270-51, KH-2/0-H/0-DJ6,3/0/L-60/150-21, PD-H-2/L-150-903.
European nomenclature codes declared: C020599,Z12050380, C020599,Z12050380,Z12050480, Z1203020302, C020501, C020401, Z1203020680.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 1 229 |
| 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 | 1 229 |
|---|---|
| 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. SORIMEX sp. z o.o. was not found in either the U.S. or the Canadian register.