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P-303

EUDAMED

Class IIb (EU MDR)

Ref P-303

by Radianqbio

Identity

Trade Name
P-303 EUDAMED
Device Name
EXTERNAL CARDIOVERSION DEFIBRILLATOR ELECTRODE PADS EUDAMED
Model / Reference
P-303 EUDAMED

Identifiers

Primary DI / UDI-DI
08809434320102 EUDAMED
Basic UDI-DI
B-08809434320102 EUDAMED
EMDN Code
C020401 EXTERNAL CARDIOVERSION DEFIBRILLATOR ELECTRODE PADS EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
Ireland EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

P-303 by Radianqbio — Class IIb — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

Manufacturer
Radianqbio
EUDAMED SRN
KR-MF-000013678
Authorised Representative
S.B. Pharma GmbH DE-AR-000005392

Sources (1)

  • EUDAMED 94962579-4462-4489-a21e-843a9c2a5b1f 61 fields · synced Jun 18, 2026