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NextAR PSI Instruments tray

by Medacta International SA

Ref 02.23.10.8201

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number764014274KSR0240N00AY Basic UDI-DIDate16 Sep 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

No notified-body 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  • Withdrawn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
Knee Instrument tray / Caddy / Support / Mat / Sterilization case
Model / Reference
02.23.10.8201
Primary DI / UDI-DI
07630971288492
Basic UDI-DI
764014274KSR0240N00AY
Direct Marketing DI
07630971288492
EMDN Code
L091199 Orthopaedic prosthetics instruments, reusable - other
Device Class
Class I
Market of Registration
Italy

Manufacturer details

EUDAMED SRN
CH-MF-000033473
Authorised representative
Medacta Italia srl IT-AR-000022505

Other devices from Medacta International SA

See all devices from Medacta International SA →

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