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Res Electrode D50 Sea/Sp

EUDAMED

Class IIb (EU MDR)

Ref AR00008471AEModel RES ELECTRODE D50 SEA/SP

by Termosalud, S.L.

Identity

Device Name
RES ELECTRODE D50 SEA/SP EUDAMED
Model / Reference
RES ELECTRODE D50 SEA/SP EUDAMED
AR00008471AE EUDAMED

Identifiers

Primary DI / UDI-DI
08436601290854 EUDAMED
Basic UDI-DI
843660129RES50E3 EUDAMED
Direct Marketing DI
08436601290854 EUDAMED
EMDN Code
Z12040203 DERMAL REGENERATION EQUIPMENT EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
Spain EUDAMED

Clinical & Handling

Sterile

No

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

Res Electrode D50 Sea/Sp by Termosalud, S.L. — Class IIb — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Termosalud, S.L.
EUDAMED SRN
ES-MF-000019177

Sources (1)

  • EUDAMED 5ab11be1-32d8-4d89-87d4-e2dd9f518559 61 fields · synced Jun 18, 2026