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Multi-pole Pulmonary Artery RF Ablation Catheter

EUDAMED

Class III (EU MDR)

Ref PM0102Model PADN30C10120, PADN35C10120, PADN37C10120, PADN40C10120, PADN45C10120, PADN50C10120Ref PM0101Ref PM0103

by Pulnovo Medical (Wuxi) Co., Ltd.

Identity

Device Name
Multi-pole Pulmonary Artery RF Ablation Catheter EUDAMED
Model / Reference
PADN30C10120, PADN35C10120, PADN37C10120, PADN40C10120, PADN45C10120, PADN50C10120 EUDAMED
PM0102 EUDAMED
PM0101 EUDAMED
PM0103 EUDAMED

Identifiers

Primary DI / UDI-DI
06974702710656 EUDAMED
06974702710649 EUDAMED
06974702710663 EUDAMED
Basic UDI-DI
697470271PMA001H2 EUDAMED
Direct Marketing DI
06974702710656 EUDAMED
06974702710649 EUDAMED
06974702710663 EUDAMED
EMDN Code
K02030199 RADIOFREQUENCY SURGERY INSTRUMENTS, SINGLE-USE - OTHER EUDAMED

Classification

Device Class
Class III EUDAMED
Market of Registration
Italy 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: Microwave ablation system probe, non-powered

Multi-pole Pulmonary Artery RF Ablation Catheter by Pulnovo Medical (Wuxi) Co., Ltd. — Class III — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Microwave ablation system probe, non-powered.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
CN-MF-000041578
Authorised Representative
BioDomi GmbH DE-AR-000016611

Sources (3)

  • EUDAMED a64659c1-d802-462c-93c5-324e623b97c0 61 fields · synced Jul 11, 2026
  • EUDAMED 469e7506-fae7-478b-ab12-c677f8efefff 61 fields · synced May 18, 2026
  • EUDAMED 276da997-a11a-40e1-bc05-fdfa532a46ae 61 fields · synced May 19, 2026