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Covered Mounted CP Stent

by NuMED, Inc. 54 variants

Ref CMCP059Model 428.1

Active European Union

CE MDR

Valid until

23 Mar 2031

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier SGS Belgium NV

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR NumberUS26/00000111 Date7 Sep 2026IssuedStatusActive expires 23 Mar 2031

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • US26/00000111 Active

    Technical documentation EU MDR

    Certifier
    SGS Belgium NV 1639
    Issued
    7 Sep 2026
    Expires
    23 Mar 2031

Coverage

1 jurisdiction

NorwayIcelandSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaLiechtensteinAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyTürkiyeCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR 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 13 Jul 2026
  • Belgium since 13 Jul 2026
  • Bulgaria since 13 Jul 2026
  • Croatia since 13 Jul 2026
  • Cyprus since 13 Jul 2026
  • Czechia since 13 Jul 2026
  • Denmark since 13 Jul 2026
  • Estonia since 13 Jul 2026
  • Finland since 13 Jul 2026
  • France since 13 Jul 2026
  • Germany since 13 Jul 2026
  • Greece since 13 Jul 2026
  • Hungary since 13 Jul 2026
  • Iceland since 13 Jul 2026
  • Ireland since 13 Jul 2026
  • Italy since 13 Jul 2026
  • Latvia since 13 Jul 2026
  • Liechtenstein since 13 Jul 2026
  • Lithuania since 13 Jul 2026
  • Luxembourg since 13 Jul 2026
  • Malta since 13 Jul 2026
  • Netherlands since 13 Jul 2026
  • Northern Ireland since 13 Jul 2026
  • Norway since 13 Jul 2026
  • Poland since 13 Jul 2026
  • Portugal since 13 Jul 2026
  • Romania since 13 Jul 2026
  • Slovakia since 13 Jul 2026
  • Slovenia since 13 Jul 2026
  • Spain since 13 Jul 2026
  • Sweden since 13 Jul 2026
  • Türkiye since 13 Jul 2026

Last checked 30 Oct 2026.

Specification

EUDAMED

Model / Reference
428.1, CMCP059
Primary DI / UDI-DI
10887714027878
Basic UDI-DI
08877141660TL
EMDN Code
P070401020199 Ptfe vascular endoprostheses, straight - other
Device Class
Class III
EU market of registration
Belgium

Manufacturer details

EUDAMED SRN
US-MF-000010948
Authorised representative
EVOMED S.L.U. ES-AR-000047116

Other devices from NuMED, Inc.

See all devices from NuMED, Inc. →

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