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NeoGen

by Energist

Ref 930-026

NeoGen (930-026) is a medical device (EU MDR Class I; EMDN category dermal regeneration equipment) made by Energist, registered in EUDAMED on 29 May 2025 (Basic UDI-DI 506044052NeoGen-NT-001P6), active as of 22 Oct 2026.

Active European Union

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Source EUDAMED, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number506044052NeoGen-NT-001P6 Basic UDI-DI 05060440520389UDI-DIDate29 May 2025RegisteredStatusActive

Official records

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device name
NeoGen Trolley
Model / reference
930-026
Primary DI / UDI-DI
05060440520389
Basic UDI-DI
506044052NeoGen-NT-001P6
Direct marketing DI
05060440520389
EMDN code
Z12040203 Dermal regeneration equipment
Device class
Class I
System or procedure pack
System which is a device in itself
EU registration type
Standard device
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)