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MatrixRIB

by Synthes GmbH 24 variants

Ref 03.501.766S, 03.501.764, 03.501.036, 03.501.038S, 04.501.007, 04.501.005S, 03.501.756S, 04.501.024.01S, 04.501.002S, 04.501.042.01, 04.501.219.01, 03.501.751, 04.501.215.01, 04.501.208.01S, 03.501.719, 04.501.212.01, 04.501.018.01S, 04.501.094, 04.501.011S, 04.501.252.01, 03.501.048S, 04.501.012, 03.501.618, 04.501.211.01S, 04.501.217.01, 04.501.094S, 04.501.010S, 61.501.101, 03.501.768S, 03.501.704, 04.501.026.05, 04.501.095, 03.501.770, 03.501.768, 04.501.020.01S, 04.501.024.01, 03.501.085S, 03.501.042, 04.501.069, 03.501.764S, 03.501.614, 03.501.709, 04.501.217.01S, 03.501.031, 60.501.012, 03.501.062, 04.501.008, 03.501.046S, 04.501.030.05, 03.501.090, 04.501.093Model Craniomaxillofacial Drill Bits, MatrixRIB Plates and Intramedullary Splints, MatrixRIB Self-tapping and Self-drilling screws, Orthopaedic Sleeves and Drill Guide, MatrixRIB Sternal Plates, MatrixRIB Intramedullary Splints, Cases for Trauma/ CMF Devices, Craniomaxillofacial and Orthopaedic Plate Holders, Craniomaxillofacial Bending Templates and Sizers

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 Number7611819a00673K9 Basic UDI-DI Date8 Sep 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  • Withdrawn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
Craniomaxillofacial Drill Bits
MatrixRIB Plates and Intramedullary Splints
MatrixRIB Self-tapping and Self-drilling screws
Orthopaedic Sleeves and Drill Guide
MatrixRIB Sternal Plates
MatrixRIB Intramedullary Splints
Cases for Trauma/ CMF Devices
Craniomaxillofacial and Orthopaedic Plate Holders
Craniomaxillofacial Bending Templates and Sizers
Model / Reference
Craniomaxillofacial Drill Bits, 03.501.766S, 03.501.764, 03.501.036, 03.501.038S, MatrixRIB Plates and Intramedullary Splints, 04.501.007, 04.501.005S, 03.501.756S, MatrixRIB Self-tapping and Self-drilling screws, 04.501.024.01S, 04.501.002S, 04.501.042.01, 04.501.219.01, Orthopaedic Sleeves and Drill Guide, 03.501.751, 04.501.215.01, 04.501.208.01S, 03.501.719, 04.501.212.01, 04.501.018.01S, MatrixRIB Sternal Plates, 04.501.094, MatrixRIB Intramedullary Splints, 04.501.011S, 04.501.252.01, 03.501.048S, 04.501.012, 03.501.618, 04.501.211.01S, 04.501.217.01, 04.501.094S, 04.501.010S, Cases for Trauma/ CMF Devices, 61.501.101, 03.501.768S, 03.501.704, 04.501.026.05, 04.501.095, 03.501.770, 03.501.768, 04.501.020.01S, 04.501.024.01, 03.501.085S, 03.501.042, 04.501.069, 03.501.764S, 03.501.614, Craniomaxillofacial and Orthopaedic Plate Holders, 03.501.709, 04.501.217.01S, 03.501.031, 60.501.012, Craniomaxillofacial Bending Templates and Sizers, 03.501.062, 04.501.008, 03.501.046S, 04.501.030.05, 03.501.090, 04.501.093
Primary DI / UDI-DI
07611819649569, 07611819649408, 07611819348813, 07611819405417, 07611819335530, 07611819341210, 07611819649514, 07611819370456, 07611819337183, 07611819354029, 07612334154774, 07611819649354, 07612334154538, 07611819675179, 07612334118653, 07611819675544, 07611819370425, 07612334105462, 07611819341272, 07612334118592, 07611819656529, 07611819335585, 07611819479203, 07612334154507, 07612334154750, 07612334105493, 07611819341265, 07611819649156, 07611819649576, 07611819649316, 07611819335752, 07612334105479, 07611819649439, 07611819649422, 07611819370432, 07611819354111, 07611819503915, 07611819348844, 07612334110640, 07611819649552, 07611819478183, 07611819649330, 07612334154767, 07611819348684, 07611819432024, 07611819348905, 07611819335547, 07611819656512, 07611819614369, 07611819614321, 07612334105455
Basic UDI-DI
7611819a00673K9, 7611819a00056JB, 7611819a00058JF, 7611819a00225JA, 7611819a00057JD, 7611819a00274JP, 7611819a00012HP, 7611819a00079JP, 7611819a00070J5
Unit of Use DI
87611819335758, 87611819614365
Direct Marketing DI
07611819348813
07611819348820
07611819649354
07612334118653
07611819348875
07611819479203
07611819649156
07611819649316
07611819478138
07611819348844
07611819478183
07611819649330
07611819348684
07611819432024
07611819348905
07611819348868
07611819614321
EMDN Code
Z12130503, P09120599, P09120601, L091001, Z12011399, L091399, L0999, Z12139099
Device Class
Class IIa
Class IIb
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 YesEUDAMEDNoEUDAMED
  • Implantable NoEUDAMEDYesEUDAMED
  • Reusable NoEUDAMEDYesEUDAMED
  • Sutures
  • CMR Substance YesEUDAMEDNoEUDAMED

Other properties (9)

  • 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