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Jx-03

by Medi̇kal 2000 Tibbi̇ Ci̇hazlar Ve İleri̇ Teknoloji̇ San. Ve Ti̇c. A.Ş.

Ref JX-03

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number86976015JX-03T3 Basic UDI-DI 08697601522745UDI-DIDate20 Oct 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Jx-03 Gynecology Examination Table
Model / Reference
JX-03
Primary DI / UDI-DI
08697601522745
Basic UDI-DI
86976015JX-03T3
EMDN Code
V080603 Treatment, diagnosis and monitoring medical beds
Device Class
Class I
EU market of registration
Portugal

Manufacturer details

EUDAMED SRN
TR-MF-000019533

Other devices from Medi̇kal 2000 Tibbi̇ Ci̇hazlar Ve İleri̇ Teknoloji̇ San. Ve Ti̇c. A.Ş.

See all devices from Medi̇kal 2000 Tibbi̇ Ci̇hazlar Ve İleri̇ Teknoloji̇ San. Ve Ti̇c. A.Ş. →

Properties

Other properties (13)

  • Sterile: No
  • Implantable: No
  • 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