Skip to content

MatrixORTHOGNATHIC LOCK Plate

by Synthes GmbH 80 variants

Ref 04.511.942, 04.511.933, 03.511.427, 03.511.383, 04.511.963, 04.511.915, 04.511.962, 03.511.424, 04.511.915S, 04.511.981S, 04.511.928, 04.511.952S, 04.511.953S, 04.511.913, 04.511.972, 04.511.971S, 04.511.986, 04.511.941, 03.511.398, 04.511.916, 68.511.001, 03.511.422, 61.511.007, 03.511.426, 04.511.910, 03.511.389, 04.511.904S, 60.511.016, 04.511.992S, 04.511.984, 04.511.912, 04.511.946, 03.511.423, 04.511.970, 03.511.390, 03.511.402, 03.511.404, 04.511.971, 03.511.406, 04.511.911S, 04.511.990, 03.511.421, 04.511.925, 03.511.385, 04.511.962S, 04.511.985S, 04.511.931, 61.511.001, 04.511.922, 04.511.325S, 04.511.961Model MatrixORTHOGNATHIC LOCK Plate, Craniomaxillofacial Bending Templates and Sizers, Cases for Trauma/ CMF Devices, MatrixORTHOGNATHIC Plate

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 Number7611819a00652JZ Basic UDI-DI Date3 Nov 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  • Withdrawn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

Trade Name
MatrixORTHOGNATHIC LOCK
MatrixORTHOGNATHIC
Device Name
MatrixORTHOGNATHIC LOCK Plate
Craniomaxillofacial Bending Templates and Sizers
Cases for Trauma/ CMF Devices
MatrixORTHOGNATHIC Plate
Model / Reference
MatrixORTHOGNATHIC LOCK Plate, 04.511.942, 04.511.933, Craniomaxillofacial Bending Templates and Sizers, 03.511.427, 03.511.383, 04.511.963, 04.511.915, 04.511.962, 03.511.424, 04.511.915S, 04.511.981S, 04.511.928, 04.511.952S, 04.511.953S, 04.511.913, 04.511.972, 04.511.971S, 04.511.986, 04.511.941, 03.511.398, 04.511.916, Cases for Trauma/ CMF Devices, 68.511.001, 03.511.422, 61.511.007, 03.511.426, 04.511.910, 03.511.389, 04.511.904S, 60.511.016, 04.511.992S, 04.511.984, 04.511.912, 04.511.946, 03.511.423, 04.511.970, 03.511.390, 03.511.402, 03.511.404, 04.511.971, 03.511.406, 04.511.911S, 04.511.990, 03.511.421, 04.511.925, 03.511.385, 04.511.962S, 04.511.985S, 04.511.931, 61.511.001, 04.511.922, MatrixORTHOGNATHIC Plate, 04.511.325S, 04.511.961
Primary DI / UDI-DI
07611819383265, 07611819383234, 07611819507722, 07611819471955, 07611819383456, 07611819385337, 07611819383449, 07611819507692, 07611819385450, 07611819385771, 07611819383180, 07611819385580, 07611819385597, 07611819385313, 07611819383548, 07611819385856, 07611819383661, 07611819383258, 07611819472204, 07611819385344, 07611819358706, 07611819507678, 07611819516403, 07611819507715, 07611819385283, 07611819472112, 07611819385528, 07611819673090, 07611819385948, 07611819383647, 07611819385306, 07611819383302, 07611819507685, 07611819383524, 07611819472129, 07611819472242, 07611819472266, 07611819383531, 07611819472280, 07611819385412, 07611819383678, 07611819507661, 07611819383159, 07611819471979, 07611819385689, 07611819385818, 07611819383210, 07611819620032, 07611819383128, 07611819360594, 07611819383432
Basic UDI-DI
7611819a00652JZ, 7611819a00070J5, 7611819a00012HP, 7611819a00650JV
Direct Marketing DI
07611819507722
07611819507692
07611819472204
07611819358706
07611819507678
07611819516403
07611819507715
07611819472112
07611819673090
07611819507685
07611819472129
07611819472242
07611819472273
07611819472280
07611819507661
07611819471979
07611819620032
EMDN Code
P09120599, Z12139099, Z12011399
Device Class
Class IIb
Class IIa
Class I
EU market of registration
Belgium

Manufacturer details

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

Other devices from Synthes GmbH

See all devices from Synthes GmbH →

Properties

  • Sterile NoEUDAMEDYesEUDAMED
  • Implantable YesEUDAMEDNoEUDAMED
  • Sutures

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