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Kombihylan

by Rompharm Company SRL EUDAMED

Active European Union

Ref KOMBIHYLANModel HIACONNAG_IAR9

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-05944728007062 Basic UDI-DIDate12 May 2022RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Expiring

Certificates: none listed in EUDAMED

Specification

EUDAMED

Device Name
Hyaluronate+Chondroitin+NAG_intraarticular
Model / Reference
HIACONNAG_IAR9, KOMBIHYLAN
Primary DI / UDI-DI
05944728007062, 05944728008762, 05944728008755, 05944728011649, 05944728010147, 05944728010116, 05944728007055, 05944728007093, 05944728011618
Basic UDI-DI
B-05944728007062, B-05944728008762, B-05944728008755, B-05944728011649, B-05944728010147, B-05944728010116, B-05944728007055, B-05944728007093, B-05944728011618
EMDN Code
P900402 Resorbable filling and reconstruction devices
Device Class
Class III
Market of Registration
Romania
Slovakia

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
  • Reprocessed NoEUDAMEDYesEUDAMED
  • Animal Tissues
Other properties (7)
  • Reusable: No
  • Contains Latex: No
  • Human-derived: No
  • Human Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No