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COBRA PzF Coronary Stent System

by CeloNova BioSciences, Inc. United States EUDAMED

Ref 170-01-30030 EMDN P0704020102

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-00879397007370 Basic UDI-DIDate14 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  • Withdrawn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 · synced 22 Oct 2026

Model / Reference
170-01-30030
Primary DI / UDI-DI
00879397007370
Basic UDI-DI
B-00879397007370
EMDN Code
P0704020102 Coated coronary stents
Device Class
Class III
Market of Registration
Netherlands

Manufacturer details

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

Other devices from Celonova Biosciences, Inc.

See all devices from Celonova Biosciences, Inc. →

Properties & raw data

Show properties, registry sources and raw records
  • Sterile
  • Implantable
Other properties (9)
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No

Sources (1)

  • EUDAMED 90279dae-0087-4c9b-8bc8-2a5c6c022983 61 fields · synced 22 Oct 2026