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HIALUROM Tendon

by Rompharm Company SRL EUDAMED

Withdrawn No longer placed on the EU market

Ref HIALUROM TendonModel HIA_T5P

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-05944728007338 Basic UDI-DIDate20 Jan 2026RegisteredStatusWithdrawn No longer placed on the EU market

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDD Withdrawn

Certificates: none listed in EUDAMED

Specification

EUDAMED

Device Name
Hyaluronate_tendon
Model / Reference
HIA_T5P, HIALUROM Tendon
Primary DI / UDI-DI
05944728007338, 05944728011328, 05944728007284, 05944728007314, 05944728007277, 05944728007291, 05944728007260, 05944728011335
Basic UDI-DI
B-05944728007338, B-05944728011328, B-05944728007284, B-05944728007314, B-05944728007277, B-05944728007291, B-05944728007260, B-05944728011335
EMDN Code
P900402 Resorbable filling and reconstruction devices
Device Class
Class III
Market of Registration
Romania
Hungary
Greece
Germany

Manufacturer details

EUDAMED SRN
RO-MF-000002517

Other devices from Rompharm Company SRL

See all devices from Rompharm Company SRL →

Properties

Show properties
  • Sterile
  • Implantable YesEUDAMEDNoEUDAMED
Other properties (9)
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No