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genXL3

by Pollogen Ltd

Ref 30010220

genXL3 (30010220) is a Class IIa device made by Pollogen Ltd, registered in EUDAMED on 4 Aug 2026 (Basic UDI-DI B-07290016586862), active as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-07290016586862 Basic UDI-DI 07290016586862UDI-DIDate4 Aug 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Device name
genXL3
Model / reference
30010220
Primary DI / UDI-DI
07290016586862
Basic UDI-DI
B-07290016586862
EMDN code
Z12040285 General medicine therapeutic treatment instruments - consumables
Device class
Class IIa
EU registration type
Legacy device (under a directive)
EU market of registration
Belgium

Manufacturer details

EUDAMED SRN
IL-MF-000031034
Authorised representative
Obelis s.a. BE-AR-000000106

Similar devices in this category

Other devices filed under GENERAL MEDICINE THERAPEUTIC TREATMENT INSTRUMENTS.

Other devices from Pollogen Ltd

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Properties

  • Supplied sterile
Other properties (11, all answered No)