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Verbandwechsel-Set

by Raguse Gesellschaft für medizinische Produkte mbH

Ref 191037BE

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, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number42501818-TD-003-I-AC-Q2 Basic UDI-DI 04250181832082UDI-DIDate9 May 2025RegisteredStatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Verbandwechsel-Set
Model / Reference
191037BE
Primary DI / UDI-DI
04250181832082
Basic UDI-DI
42501818-TD-003-I-AC-Q2
EMDN Code
V0599 Clinical procedures kits not included in other classes - other
Device Class
Class I
Medical Purpose
Behandlungseinheit für den OP-Bereich der Allgemeinchirurgie.

Manufacturer details

EUDAMED SRN
DE-PR-000018911

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Properties

Other properties (1)

  • Sterile: No