Skip to content

Anaconda Contralateral Guiding Catheter

by Vascutek Ltd

Ref CLGC/01

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-05037881004990 Basic UDI-DI 05037881004990UDI-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  • Withdrawn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 15 Nov 2018
  • Belgium since 15 Nov 2018
  • Bulgaria since 15 Nov 2018
  • Croatia since 15 Nov 2018
  • Cyprus since 15 Nov 2018
  • Czechia since 15 Nov 2018
  • Denmark since 15 Nov 2018
  • Estonia since 15 Nov 2018
  • Finland since 15 Nov 2018
  • France since 15 Nov 2018
  • Germany since 15 Nov 2018
  • Greece since 15 Nov 2018
  • Hungary since 15 Nov 2018
  • Iceland since 15 Nov 2018
  • Ireland since 15 Nov 2018
  • Italy since 15 Nov 2018
  • Latvia since 15 Nov 2018
  • Liechtenstein since 15 Nov 2018
  • Lithuania since 15 Nov 2018
  • Luxembourg since 15 Nov 2018
  • Malta since 15 Nov 2018
  • Netherlands since 15 Nov 2018
  • Northern Ireland since 15 Nov 2018
  • Norway since 15 Nov 2018
  • Poland since 15 Nov 2018
  • Portugal since 15 Nov 2018
  • Romania since 15 Nov 2018
  • Slovakia since 15 Nov 2018
  • Slovenia since 15 Nov 2018
  • Spain since 15 Nov 2018
  • Sweden since 15 Nov 2018
  • Türkiye since 15 Nov 2018

Last checked 31 Oct 2026.

Specification

EUDAMED

Device Name
ANACONDA™ AAA Stent Graft System
Model / Reference
CLGC/01
Primary DI / UDI-DI
05037881004990
Basic UDI-DI
B-05037881004990
EMDN Code
P0780 Vascular and cardiac prostheses - accessories
Device Class
Class III
EU market of registration
Belgium

Manufacturer details

EUDAMED SRN
GB-MF-000003643
Authorised representative
TERUMO EUROPE N.V. BE-AR-000001433

Other devices from Vascutek Ltd.

See all devices from Vascutek Ltd. →

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