Skip to content

Evolution Mpx™ Tibial Insert

by Suzhou MicroPort OrthoRecon Co., Ltd 180 variants

Ref 4233712Model 4233110、4243110、4233112、4243112、4233114、4243114、4233117、4243117、4233120

Active European Union

CE MDR

Valid until

19 Feb 2031

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier TÜV SÜD Product Service GmbH

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 Number69416351110101021EMPXTIWP Basic UDI-DI 06941635108881UDI-DIDate23 Jun 2026RegisteredStatusActive

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Model / Reference
4233110、4243110、4233112、4243112、4233114、4243114、4233117、4243117、4233120, 4233712
Primary DI / UDI-DI
06941635108881
Basic UDI-DI
69416351110101021EMPXTIWP
EMDN Code
P090903020202 Bicompartmental primary implant fixed bearing tibial inserts
Device Class
Class III
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
CN-MF-000001566
Authorised representative
MicroPort Medical B.V. NL-AR-000000166

Other devices from Suzhou Microport Orthorecon Co., Ltd.

See all devices from Suzhou Microport Orthorecon Co., Ltd. →

Properties

  • 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