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NeoGen Footswitch

EUDAMED

Class I (EU MDR)

Ref 230-027

by Energist

Identity

Trade Name
NeoGen Footswitch EUDAMED
NeoGen EUDAMED
Device Name
NeoGen Footswitch EUDAMED
Model / Reference
230-027 EUDAMED

Identifiers

Primary DI / UDI-DI
05060440520365 EUDAMED
Basic UDI-DI
506044052NeoGen-NF-001JC EUDAMED
B-05060440520365 EUDAMED
EMDN Code
Z12040203 DERMAL REGENERATION EQUIPMENT EUDAMED

Classification

Device Class
Class I EUDAMED
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

NeoGen Footswitch by Energist — Class I — MDD, MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Energist
EUDAMED SRN
GB-MF-000021765
Authorised Representative
Advena Limited MT-AR-000000234

Sources (2)

  • EUDAMED 0903a29e-a6b8-4175-9f1d-43e83e5758fd 61 fields · synced Jun 19, 2026
  • EUDAMED 01e11982-db25-409f-95a2-647aea1e5c80 61 fields · synced May 17, 2026