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ViscoPhi %2.2

by Phibio GmbH Germany EUDAMED

Ref PHI222DE-VSP

EMDN P900402

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number1TD-MDR-0076/10/2025 Date25 Feb 2026IssuedStatusActive expires 1 Oct 2028

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 Issued

    Technical documentation EU MDR

    Notified body
    Notified body 2764
    Issued
    25 Feb 2026
    Expires
    1 Oct 2028

Specification

EUDAMED · synced 22 Oct 2026

Device Name
Sterile Hyaluronic Acid Intra-Articular Gel Implant
Model / Reference
PHI222DE-VSP
Primary DI / UDI-DI
04250906200509
Basic UDI-DI
42509062IALSQ
Direct Marketing DI
04250906200509
EMDN Code
P900402 Resorbable filling and reconstruction devices
Device Class
Class III
Market of Registration
Germany

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 6a74aab6-854d-486e-a84f-5ee8dd338b42 61 fields · synced 22 Oct 2026