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Ultrapro

by Johnson & Johnson International 11 variants

Ref UHSOV1Model ULTRAPRO Hernia System

Active European Union

CE MDR

Valid until

7 Jan 2031

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier BSI Group The Netherlands B.V.

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 7 Nov 2026. What this means

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR NumberMDR 730049 Date8 Jan 2026IssuedStatusActive expires 7 Jan 2031

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • MDR 730049 Active Reissued

    Technical documentation EU MDR

    Certifier
    BSI Group The Netherlands B.V. 2797
    Issued
    8 Jan 2026
    Expires
    7 Jan 2031

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
ULTRAPRO Hernia System
Model / Reference
ULTRAPRO Hernia System, UHSOV1
Primary DI / UDI-DI
10705031085848
Basic UDI-DI
0705031a0000943
EMDN Code
P900204 Surgical meshes, more than one component
Device Class
Class III
EU 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

  • 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