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ZFace

by Zimmer MedizinSysteme GmbH

Ref 5811Model ZFace

ZFace (5811) is a Class IIa device made by Zimmer MedizinSysteme GmbH, registered in EUDAMED on 29 Oct 2026 (Basic UDI-DI 4053815D5811DZ), active as of 7 Nov 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 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number4053815D5811DZ Basic UDI-DI 04053815982340UDI-DIDate29 Oct 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device name
ZFace UMS-01
Model / reference
ZFace, 5811
Primary DI / UDI-DI
04053815982340
Basic UDI-DI
4053815D5811DZ
Direct marketing DI
04053815982340
EMDN code
Z120602 Physiotherapy equipment
Device class
Class IIa
EU registration type
Standard device
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000006141

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Properties

Other properties (14, all answered No)