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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Organization name
UDI-DI code
Reference / catalog number

Ablation electrode — Class III MDR by HAGMED Sp. z o.o. Sp.…

MD Atlas
HAGMED Sp. z o.o. Sp. komandytowa

EUDAMED last updated this device on Oct 27, 2025

Ablation electrode

590067269EAUJ

On the marketClass III

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: HAGMED Sp. z o.o. Sp. komandytowa
UDI-DI code: 05907645810887
Reference / catalog number: EA7QS252U4I8AT

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View device family (Basic UDI)

Manufacturer information

Organization name: HAGMED Sp. z o.o. Sp. komandytowa
SRN: PL-MF-000021862
Manufacturer status: Active

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW010
EUDAMED did not publish a description for this code.

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Market distribution

Primary placement in Poland; available across 2 countries total.

Country	On market since	Until
PolandPrimary placement	Jan 4, 2021	Still on market
Malta	Jan 2, 2026	Still on market

Device identification

Trade name: Ablation electrode
UDI-DI code: 05907645810887
Basic UDI-DI: 590067269EAUJ
Reference / catalog number: EA7QS252U4I8AT
Issuing entity: GS1

Classification

Risk category: Class III
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)05907645810887

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UDI-PI DataMatrix

The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.

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EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

C020301ARRHYTHMOGENIC FOCI RADIOFREQUENCY ABLATION CATHETERS

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

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Certificates

Certificate health across this manufacturer's portfolio.

1434-MDR-020/2025Issued
Quality management systemNotified body: 1434Expiry: Oct 9, 2030
1434-MDR-019/2025Issued
Technical documentationNotified body: 1434Expiry: Oct 9, 2030