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Restore Plus Dcb

by Cardionovum GmbH 39 variants

Ref RP 2.25-20

Active European Union

CE MDD

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/MDD NumberB-05906190154125 Basic UDI-DI 05906190154125UDI-DIDate24 Aug 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

NorwayIcelandSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaLiechtensteinAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyTürkiyeCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDD Active

EU market availability

Made available in 32 countries, as listed in EUDAMED:

Declared by the manufacturer in EUDAMED for this device version; may not cover every market.

  • Austria since 24 May 2021
  • Belgium since 24 May 2021
  • Bulgaria since 24 May 2021
  • Croatia since 24 May 2021
  • Cyprus since 24 May 2021
  • Czechia since 24 May 2021
  • Denmark since 24 May 2021
  • Estonia since 24 May 2021
  • Finland since 24 May 2021
  • France since 24 May 2021
  • Germany since 24 May 2021
  • Greece since 24 May 2021
  • Hungary since 24 May 2021
  • Iceland since 24 May 2021
  • Ireland since 24 May 2021
  • Italy since 24 May 2021
  • Latvia since 24 May 2021
  • Liechtenstein since 24 May 2021
  • Lithuania since 24 May 2021
  • Luxembourg since 24 May 2021
  • Malta since 24 May 2021
  • Netherlands since 24 May 2021
  • Northern Ireland since 24 May 2021
  • Norway since 24 May 2021
  • Poland since 24 May 2021
  • Portugal since 24 May 2021
  • Romania since 24 May 2021
  • Slovakia since 24 May 2021
  • Slovenia since 24 May 2021
  • Spain since 24 May 2021
  • Sweden since 24 May 2021
  • Türkiye since 24 May 2021

Last checked 30 Oct 2026.

Specification

EUDAMED

Device Name
RESTORE PLUS DCB Paclitaxel Releasing PTCA Balloon Catheter
Model / Reference
RP 2.25-20
Primary DI / UDI-DI
05906190154125
Basic UDI-DI
B-05906190154125
EMDN Code
C010401020101 Ptca balloon dilation catheters
Device Class
Class III
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000005316

Other devices from Cardionovum GmbH

See all devices from Cardionovum GmbH →

Properties

  • Sterile
  • Incorporates Medicinal Product

Other properties (9)

  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No