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COBRA PzF Coronary Stent System

by CeloNova BioSciences, Inc. EUDAMED

Active European Union

Ref 170-01-35030

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-00879397007431 Basic UDI-DIDate15 Feb 2022RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDD Expiring

Certificates: none listed in EUDAMED

Specification

EUDAMED

Model / Reference
170-01-35030
Primary DI / UDI-DI
00879397007431
Market of Registration
Netherlands

Manufacturer details

EUDAMED SRN
US-MF-000008827
Authorised representative
Emergo Europe B.V. NL-AR-000000116

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