Skip to content

Universal-Set

by Fuhrmann GmbH 8 variants

Ref 38179

Active European Union

CE MDR

Valid until

Not listed

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

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number405485838179D7 Basic UDI-DI 04054858028316UDI-DIDate21 Apr 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Model / Reference
38179
Primary DI / UDI-DI
04054858028316
Basic UDI-DI
405485838179D7
EMDN Code
V0599 Clinical procedures kits not included in other classes - other
Device Class
Class IIa
Medical Purpose
Set für operative Eingriffe, fachabteilungsübergreifend

Manufacturer details

EUDAMED SRN
DE-PR-000019607

Related devices

Category: Ophthalmic surgical procedure kit, non-medicated, single-use

Other devices from Fuhrmann GmbH

See all devices from Fuhrmann GmbH →

Properties

  • Sterile