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NeoGen Footswitch

by Energist

Ref 230-027

NeoGen Footswitch (230-027) is a medical device (EU MDD Class I; EU MDD Class IIb; EMDN category dermal regeneration equipment) made by Energist, registered in EUDAMED on 14 Apr 2026 (Basic UDI-DI 506044052NeoGen-NF-001JC), active as of 22 Oct 2026.

Active European Union

CE MDR CE MDD

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD Number506044052NeoGen-NF-001JC Basic UDI-DI 05060440520365UDI-DIDate14 Apr 2026RegisteredStatusActive
European UnionCE/MDR Number506044052NeoGen-NF-001JC Basic UDI-DI 05060440520365UDI-DIDate14 Apr 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDD, CE/MDR Active

Specification

EUDAMED

Trade name
NeoGen Footswitch
NeoGen
Model / reference
230-027
Primary DI / UDI-DI
05060440520365
Basic UDI-DI
506044052NeoGen-NF-001JC, B-05060440520365
EMDN code
Z12040203 Dermal regeneration equipment
Device class
Class I
Class IIb
EU registration type
Standard device
Legacy device (under a directive)
EU market of registration
Netherlands

Manufacturer details

EUDAMED SRN
GB-MF-000021765
Authorised representative
Advena Limited MT-AR-000000234

Similar devices in this category

Other devices filed under DERMAL REGENERATION EQUIPMENT.

Other devices from Energist

Properties

Other properties (14, all answered No)