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Sterile Hyaluronic Acid Intra-Articular Gel Implant

by KLC Biyoteknoloji ve Dış Ticaret Anonim Şirketi

Ref KLC-L-0505

Active European Union

CE MDR

Valid until

9 Jun 2029

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier Notice Belgelendirme, Muayene ve Denetim Hizmetleri Anonim Şirketi

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number868394142901LNR6R Basic UDI-DI 08683941429516UDI-DIDate15 Jun 2026RegisteredStatusActive

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • 1TD-MDR-0043/06/2026/01 Active

    Technical documentation EU MDR

    Certifier
    Notice Belgelendirme, Muayene ve Denetim Hizmetleri Anonim Şirketi 2764
    Issued
    10 Jun 2026
    Expires
    9 Jun 2029

Coverage

1 jurisdiction

Türkiye
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

  • Türkiye

Specification

EUDAMED

Device Name
Sterile Hyaluronic Acid Intra-Articular Gel Implant Linear
Model / Reference
KLC-L-0505
Primary DI / UDI-DI
08683941429516
Basic UDI-DI
868394142901LNR6R
EMDN Code
P900402 Resorbable filling and reconstruction devices
Device Class
Class III
EU market of registration
Türkiye

Manufacturer details

EUDAMED SRN
TR-MF-000042036

Other devices from KLC Biyoteknoloji ve Dış Ticaret Anonim Şirketi

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