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ReCure® elektrodepad

EUDAMED

Class IIb (EU MDR)

Ref PAD-003Model EXA-001

by Aneuvo

Identity

Trade Name
ReCure® elektrodepad EUDAMED
Device Name
ExaStim Stimulation System EUDAMED
Model / Reference
EXA-001 EUDAMED
PAD-003 EUDAMED

Identifiers

Primary DI / UDI-DI
00850053287046 EUDAMED
Basic UDI-DI
0850053287EXSYYU EUDAMED
EMDN Code
Z120601 ELECTROTHERAPY EQUIPMENT (INCLUDED TENS) EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
Netherlands 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

ReCure® elektrodepad by Aneuvo — 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
Aneuvo
EUDAMED SRN
US-MF-000041520
Authorised Representative
Obelis s.a. BE-AR-000000106

Sources (1)

  • EUDAMED 2906f203-c5a7-4eb8-a683-0c98e3531a03 61 fields · synced Jul 9, 2026