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COPERNIC Temporary occlusion catheter

by Balt extrusion SAS EUDAMED

Active European Union

Ref COPERNIC15

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-03700481332429 Basic UDI-DIDate5 Oct 2026RegisteredStatusActive

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  • Withdrawn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 4 Mar 1998
  • Belgium since 4 Mar 1998
  • Bulgaria since 4 Mar 1998
  • Croatia since 4 Mar 1998
  • Cyprus since 4 Mar 1998
  • Czechia since 4 Mar 1998
  • Denmark since 4 Mar 1998
  • Estonia since 4 Mar 1998
  • Finland since 4 Mar 1998
  • France since 4 Mar 1998
  • Germany since 4 Mar 1998
  • Greece since 4 Mar 1998
  • Hungary since 4 Mar 1998
  • Iceland since 4 Mar 1998
  • Ireland since 4 Mar 1998
  • Italy since 4 Mar 1998
  • Latvia since 4 Mar 1998
  • Liechtenstein since 4 Mar 1998
  • Lithuania since 4 Mar 1998
  • Luxembourg since 4 Mar 1998
  • Malta since 4 Mar 1998
  • Netherlands since 4 Mar 1998
  • Northern Ireland since 4 Mar 1998
  • Norway since 4 Mar 1998
  • Poland since 4 Mar 1998
  • Portugal since 4 Mar 1998
  • Romania since 4 Mar 1998
  • Slovakia since 4 Mar 1998
  • Slovenia since 4 Mar 1998
  • Spain since 4 Mar 1998
  • Sweden since 4 Mar 1998
  • Türkiye since 4 Mar 1998

Last checked 27 Oct 2026.

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.

Specification

EUDAMED

Device Name
COPERNIC Temporary occlusion catheter
Model / Reference
COPERNIC15
Primary DI / UDI-DI
03700481332429
Basic UDI-DI
B-03700481332429
EMDN Code
C01020101 Central i.v. single-lumen catheters, peripheral access
Device Class
Class III
Market of Registration
France

Manufacturer details

EUDAMED SRN
FR-MF-000007563

Other devices from Balt extrusion SAS

See all devices from Balt extrusion SAS →

Properties

  • Sterile

Other properties (12)

  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No