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Phagenyx

by Phagenesis Ltd

Ref EPSB4

Phagenyx (EPSB4) is a medical device (EU MDR Class IIa; EMDN category neurological stimulators) made by Phagenesis Ltd, registered in EUDAMED on 13 Aug 2026 (Basic UDI-DI 0506045348B44N), active as of 24 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 linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, synced 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number0506045348B44N Basic UDI-DI 05060453480052UDI-DIDate13 Aug 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device name
Phagenyx Base Station
Model / reference
EPSB4
Primary DI / UDI-DI
05060453480052
Basic UDI-DI
0506045348B44N
Direct marketing DI
05060453480052
EMDN code
Z12101106 Neurological stimulators
Device class
Class IIa
EU registration type
Standard device
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
GB-MF-000015848
Authorised representative
Veranex Germany GmbH DE-AR-000005578

Similar devices in this category

Other devices filed under NEUROLOGICAL STIMULATORS.

Other devices from Phagenesis Ltd

  • Phagenyx

    Class IIa
  • Phagenyx

    Class IIa

Properties

Other properties (14, all answered No)