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MYNX CONTROL™ Vascular Closure Device 5F

by Cordis US Corp. United States EUDAMED

Ref MX5060E EMDN H900304

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number07050320000000000000041CF Basic UDI-DIDate17 Jun 2024RegisteredStatusActive

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  • Withdrawn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 771922 Supplemented

    Technical documentation EU MDR

    Notified body
    Notified body 2797
    Issued
    11 Jun 2026
    Expires
    22 Apr 2029
    Reason
    Change approved

Specification

EUDAMED · synced 25 Oct 2026

Device Name
MYNX CONTROL™ Vascular Closure Device
Model / Reference
MX5060E
Primary DI / UDI-DI
10862028000441
Basic UDI-DI
07050320000000000000041CF
EMDN Code
H900304 Plugs
Device Class
Class III
Market of Registration
Ireland

Manufacturer details

EUDAMED SRN
US-MF-000020031
Authorised representative
Cordis Cashel IE-AR-000017793

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Properties & raw data

Show properties, registry sources and raw records
  • 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

Sources (1)

  • EUDAMED 10862028000441|07050320000000000000041CF 61 fields · synced 25 Oct 2026