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NeoGen

by Energist

Ref 930-025

NeoGen (930-025) is a medical device (EU MDD Class IIb; EMDN category dermal regeneration equipment) made by Energist, registered in EUDAMED on 7 Apr 2022 (Basic UDI-DI B-05060440520358), active as of 22 Oct 2026.

Active European Union

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 NumberB-05060440520358 Basic UDI-DI 05060440520358UDI-DIDate7 Apr 2022RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Device name
NeoGen PSR Trolley Black
Model / reference
930-025
Primary DI / UDI-DI
05060440520358
Basic UDI-DI
B-05060440520358
EMDN code
Z12040203 Dermal regeneration equipment
Device class
Class IIb
EU registration type
Legacy device (under a directive)
EU market of registration
France

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 (12, all answered No)