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Jonexa Up 2.0 %

by i+Med S.Coop. Spain EUDAMED

Ref PV00091Model Jonexa Up 2.0 % EMDN P900402

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08056515860761 Basic UDI-DIDate4 Mar 2026RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Expiring

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • 2026 DR 0071 Issued

    Technical documentation EU MDR

    Notified body
    Notified body 0318
    Issued
    5 Feb 2026
    Expires
    26 Jun 2029

Specification

EUDAMED · synced 24 Oct 2026

Trade Name
Jonexa Up 2.0 %
Jonexa UP
Device Name
Viscosuplemento intraarticular entrecruzado (LBTRA)
Model / Reference
Jonexa Up 2.0 %, PV00091
Primary DI / UDI-DI
08056515860761
Basic UDI-DI
B-08056515860761, 8437015992TR00782
EMDN Code
P900402 Resorbable filling and reconstruction devices
Device Class
Class III
Market of Registration
Italy

Manufacturer details

EUDAMED SRN
ES-MF-000008633

Other devices from i+Med S.Coop.

See all devices from i+Med S.Coop. →

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 (2)

  • EUDAMED 9f25eab8-54b5-4fde-8a04-ec3f7499f901 61 fields · synced 22 Oct 2026
  • EUDAMED 08056515860761|8437015992TR00782 61 fields · synced 24 Oct 2026