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Universal-Set

by Raguse Gesellschaft für medizinische Produkte mbH 2 variants

Ref 569703OPBE

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number42501818-TD-003-IIa-FE-B8 Basic UDI-DIDate24 Jun 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  • Withdrawn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

Device Name
OP-Sets Behandlungseinheit - Fachübergreifende Einsatzgebiete - IIa
Model / Reference
569703OPBE
Primary DI / UDI-DI
04255575130263
Basic UDI-DI
42501818-TD-003-IIa-FE-B8
EMDN Code
V0599 Clinical procedures kits not included in other classes - other
Device Class
Class IIa
Medical Purpose
OP-Sets Behandlungseinheit - Fachübergreifende Einsatzgebiete

Manufacturer details

EUDAMED SRN
DE-PR-000018911

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Properties

Other properties (1)

  • Sterile: No