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MatrixWAVE

by Synthes GmbH 2 variants

Ref 04.503.821, 60.590.004, 68.590.054, 68.590.057, 68.590.050, 04.503.820, 68.590.055, 03.503.049, 04.503.824.05, 04.503.825.01, 68.590.053, 04.503.824.01Model MatrixWAVE MMF Plate, Cases for Trauma/ CMF Devices, Matrix Wave Application Instruments, MatrixWAVE MMF Screw

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 linked in EUDAMED

A group certificate may exist

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 Number7611819a00787KR Basic UDI-DI Date30 Jul 2025RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
MatrixWAVE MMF Plate
Cases for Trauma/ CMF Devices
Matrix Wave Application Instruments
MatrixWAVE MMF Screw
Model / Reference
MatrixWAVE MMF Plate, 04.503.821, Cases for Trauma/ CMF Devices, 60.590.004, 68.590.054, 68.590.057, 68.590.050, 04.503.820, 68.590.055, Matrix Wave Application Instruments, 03.503.049, MatrixWAVE MMF Screw, 04.503.824.05, 04.503.825.01, 68.590.053, 04.503.824.01
Primary DI / UDI-DI
07612334093509, 07612334092625, 07612334094759, 07612334094780, 07612334093516, 07612334093493, 07612334094766, 07612334093486, 07612334093462, 07612334104540, 07612334093547, 07612334104533
Basic UDI-DI
7611819a00787KR, 7611819a00012HP, 7611819a00101HP, 7611819a00788KT
Unit of Use DI
87612334093468
Direct Marketing DI
07612334092625
07612334094759
07612334094780
07612334093516
07612334094766
07612334093486
07612334093547
EMDN Code
P09120599, Z12011399, P091299, P09120601
Device Class
Class IIb
Class I
EU market of registration
Belgium

Manufacturer details

EUDAMED SRN
CH-MF-000013345
Authorised representative
DePuy Ireland UC IE-AR-000009328

Related devices

Category: Orthopaedic fixation plate, non-bioabsorbable

Other devices from Synthes GmbH

See all devices from Synthes GmbH →

Properties

  • Implantable YesEUDAMEDNoEUDAMED
  • Reusable NoEUDAMEDYesEUDAMED
  • Sutures
  • CMR Substance NoEUDAMEDYesEUDAMED

Other properties (10)

  • Sterile: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No