Identity
- Trade Name
- Ablation electrode EUDAMED
- Device Name
- Abliation electrodes EA EUDAMED
- Model / Reference
- EA7QS252U4I8AT EUDAMED
Identifiers
- Primary DI / UDI-DI
- 05907645810887 EUDAMED
- Basic UDI-DI
- 590067269EAUJ EUDAMED
- Direct Marketing DI
- 05907645810887 EUDAMED
- EMDN Code
- C020301 ARRHYTHMOGENIC FOCI RADIOFREQUENCY ABLATION CATHETERS EUDAMED
Classification
- Device Class
- Class III EUDAMED
- Market of Registration
- Poland EUDAMED
Clinical & Handling
Sterile
Yes
EUDAMED
Implantable
No
EUDAMED
Reusable
No
EUDAMED
Contains Latex
No
EUDAMED
Reprocessed
No
EUDAMED
CMR Substance
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Ablation electrode by HAGMED Sp. z o.o. Sp. komandytowa — Class III — MDR — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/MDR
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 590067269EAUJ | Class III | Active |
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Manufacturer
- Manufacturer
- HAGMED Sp. z o.o. Sp. komandytowa
- EUDAMED SRN
- PL-MF-000021862
Sources (1)
- EUDAMED acd45423-c578-41b6-9a71-05b34a85d4d5 61 fields · synced Jun 18, 2026