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Ablation electrode

EUDAMED

Class III (EU MDR)

Ref EA7QL252U8AT

by HAGMED Sp. z o.o. Sp. komandytowa

Identity

Trade Name
Ablation electrode EUDAMED
Device Name
Abliation electrodes EA EUDAMED
Model / Reference
EA7QL252U8AT EUDAMED

Identifiers

Primary DI / UDI-DI
05900672696516 EUDAMED
Basic UDI-DI
590067269EAUJ EUDAMED
Direct Marketing DI
05900672696516 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

Category: Cardiac radio-frequency ablation system catheter

Ablation electrode by HAGMED Sp. z o.o. Sp. komandytowa — Class III — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Cardiac radio-frequency ablation system catheter.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
HAGMED Sp. z o.o. Sp. komandytowa
EUDAMED SRN
PL-MF-000021862

Sources (1)

  • EUDAMED 6cc68bce-e0b4-49ce-81ce-f1edb5039f87 61 fields · synced Jun 18, 2026