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GORE-TEX® Stretch Vascular Graft

by W. L. Gore & Associates, Inc. EUDAMED

Active European Union

Ref SRRT06030040LEModel GORE-TEX® Vascular Graft

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number0733132200623902L Basic UDI-DIDate5 May 2026RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • MDR 732281 Reissued

    Technical documentation EU MDR

    Notified body
    Notified body 2797
    Issued
    20 Jul 2026
    Expires
    19 Jul 2031

Specification

EUDAMED

Device Name
GORE-TEX® Vascular Graft
Model / Reference
GORE-TEX® Vascular Graft, SRRT06030040LE
Primary DI / UDI-DI
00733132656790
Basic UDI-DI
0733132200623902L
EMDN Code
P070102020102 Ptfe vascular prostheses, straight, reinforced
Device Class
Class III
Market of Registration
Netherlands

Manufacturer details

EUDAMED SRN
US-MF-000001141
Authorised representative
W.L. Gore & Associates B.V. NL-AR-000000168

Other devices from W. L. Gore & Associates, Inc.

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Properties

Show properties
  • Sterile
  • Implantable
Other properties (11)
  • 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