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H-52 Egyoldali Gumiöves Lágyéksérvkötő /Jobb/75

by PRIMA-PROTETIKA Gyártó és Kereskedelmi Korlátolt Felelősségű Társaság

Ref 2004971521075Model H-52 EGYOLDALI LÁGYÉKSÉRVKÖTŐ

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number59989941PPHAS-0063-94 Basic UDI-DI 05998994133505UDI-DIDate30 Sep 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Model / Reference
H-52 EGYOLDALI LÁGYÉKSÉRVKÖTŐ, 2004971521075
Primary DI / UDI-DI
05998994133505
Basic UDI-DI
59989941PPHAS-0063-94
EMDN Code
Y060406 Abdominal hernia supports
Device Class
Class I
EU market of registration
Hungary

Manufacturer details

EUDAMED SRN
HU-MF-000003677

Other devices from PRIMA-PROTETIKA Gyártó és Kereskedelmi Korlátolt Felelősségű Társaság

See all devices from PRIMA-PROTETIKA Gyártó és Kereskedelmi Korlátolt Felelősségű Társaság →

Properties

Other properties (13)

  • Sterile: No
  • Implantable: No
  • 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