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Intergard Synergy Knitted Ultrathin

by Intervascular SAS 15 variants

Ref IGKUT0008RS15-40SG

Active European Union

CE MDR

Valid until

26 Mar 2031

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier TÜV SÜD Product Service GmbH

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number0384401013833S Basic UDI-DI 00384401013457UDI-DIDate11 Jun 2026RegisteredStatusActive

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Intergard Synergy Antimicrobial Collagen Coated Vascular Grafts
Model / Reference
IGKUT0008RS15-40SG
Primary DI / UDI-DI
00384401013457
Basic UDI-DI
0384401013833S
EMDN Code
P070102010101 Dacron vascular prostheses, straight, knitted
Device Class
Class III
EU market of registration
France

Manufacturer details

EUDAMED SRN
FR-MF-000002878

Other devices from Intervascular SAS

See all devices from Intervascular SAS →

Properties

  • Sterile
  • Implantable
  • Animal Tissues
  • Incorporates Medicinal Product

Other properties (9)

  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No