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Ultrapro

by Johnson & Johnson International Belgium EUDAMED

Ref UMS1Model ULTRAPRO

EMDN P900204

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number0705031a014524X Basic UDI-DIDate17 Nov 2025RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Not covered

European Union — CE/MDR Active

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • MDR 730047 Reissued

    Technical documentation EU MDR

    Notified body
    Notified body 2797
    Issued
    2 Feb 2026
    Expires
    1 Feb 2031

Specification

EUDAMED · synced 24 Oct 2026

Device Name
ULTRAPRO Mesh
Model / Reference
ULTRAPRO, UMS1
Primary DI / UDI-DI
10705031085930
Basic UDI-DI
0705031a014524X
EMDN Code
P900204 Surgical meshes, more than one component
Device Class
Class III
Market of Registration
Belgium

Manufacturer details

EUDAMED SRN
BE-MF-000008018

Other devices from Johnson & Johnson International

See all devices from Johnson & Johnson International →

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 10705031085930|0705031A014524X 61 fields · synced 24 Oct 2026