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Artro DC

by Phibio GmbH Germany EUDAMED

Ref PHI222DE-ARTModel 0.5ml - 1ml - 1.5ml - 2ml - 2.5ml - 3ml - 4ml - 5ml

EMDN P900402

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number426035399LNRL Basic UDI-DIDate7 Oct 2025RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Not covered

European Union — CE/MDR Active

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • 1TD-MDR-0076/10/2025 Withdrawn

    Technical documentation EU MDR

    Notified body
    Notified body 2764
    Issued
    2 Oct 2025
    Expires
    1 Oct 2028
    Reason
    Not on market

Specification

EUDAMED · synced 22 Oct 2026

Device Name
Sterile Hyaluronic Acid Intra-Articular Gel Implant
Model / Reference
0.5ml - 1ml - 1.5ml - 2ml - 2.5ml - 3ml - 4ml - 5ml, PHI222DE-ART
Primary DI / UDI-DI
04260353992131
Basic UDI-DI
426035399LNRL
EMDN Code
P900402 Resorbable filling and reconstruction devices
Device Class
Class III
Market of Registration
Türkiye

Manufacturer details

EUDAMED SRN
DE-MF-000045435

Other devices from Phibio GmbH

See all devices from Phibio GmbH →

Properties & raw data

Show properties, registry sources and raw records
  • 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

Sources (1)

  • EUDAMED 4bf0fa47-1578-47d4-aba0-5082194f2302 61 fields · synced 22 Oct 2026