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Matrix

by Synthes GmbH 425 variants

Ref 04.633.191, 04.634.550, 04.639.135, 04.639.850, 04.639.430S, 04.606.965, 04.634.155, 04.639.945, 04.606.620S, 04.639.960, 04.651.070S, 03.511.375, 04.632.750S, 04.616.950S, 04.633.326, 04.606.650S, 04.633.279, 09.633.192S, 04.651.075, 04.632.835, 04.632.635, 04.634.125, 04.634.835, 04.632.640, 04.616.135, 04.632.160S, 04.616.630, 04.651.235S, 04.632.850S, 09.633.190S, 04.606.945S, 04.651.505, 03.511.370, 04.632.640S, 04.633.330, 04.606.630, 04.639.155S, 04.651.600, 04.651.430, 04.632.620, 04.651.275, 04.651.320S, 04.634.425, 04.651.520, 04.606.745S, 04.632.855S, 04.633.282S, 04.632.835S, 04.616.940, 04.616.665, 04.616.185Model Connecting Rods for Spine Connecting Rod, Matrix Spine Bone Screw, Posterior Rods for Spine MIS Rods Ø 5.5mm, Craniomaxillofacial Bending Templates and Sizers, Posterior Connectors for Spine Snap-On Transverse Connector, Posterior Rods for Spine Rod Ø 5.5mm, Posterior Rods for Spine Cobalt Chrome Rod Ø 5.5mm

Active European Union

CE MDR

Valid until

No date given

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 Number7611819a00441JJ Basic UDI-DI Date8 Aug 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  • Withdrawn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
Connecting Rod
Matrix Pedicle Screw Polyaxial Cannulated Reduction Screw
MIS Rod Ø 5.5mm
Craniomaxillofacial Bending Templates and Sizers
Snap-On Transverse Connector
Rod Ø 5.5mm
Cobalt Chrome Rod Ø 5.5mm
Model / reference
Connecting Rods for Spine Connecting Rod, 04.633.191, Matrix Spine Bone Screw, 04.634.550, 04.639.135, 04.639.850, 04.639.430S, 04.606.965, 04.634.155, 04.639.945, 04.606.620S, 04.639.960, Posterior Rods for Spine MIS Rods Ø 5.5mm, 04.651.070S, Craniomaxillofacial Bending Templates and Sizers, 03.511.375, 04.632.750S, 04.616.950S, Posterior Connectors for Spine Snap-On Transverse Connector, 04.633.326, 04.606.650S, Posterior Rods for Spine Rod Ø 5.5mm, 04.633.279, Posterior Rods for Spine Cobalt Chrome Rod Ø 5.5mm, 09.633.192S, 04.651.075, 04.632.835, 04.632.635, 04.634.125, 04.634.835, 04.632.640, 04.616.135, 04.632.160S, 04.616.630, 04.651.235S, 04.632.850S, 09.633.190S, 04.606.945S, 04.651.505, 03.511.370, 04.632.640S, 04.633.330, 04.606.630, 04.639.155S, 04.651.600, 04.651.430, 04.632.620, 04.651.275, 04.651.320S, 04.634.425, 04.651.520, 04.606.745S, 04.632.855S, 04.633.282S, 04.632.835S, 04.616.940, 04.616.665, 04.616.185
Primary DI / UDI-DI
07611819346338, 07611819345058, 07611819429802, 07611819378759, 07611819470873, 07611819344075, 07611819344914, 07611819378872, 07611819479319, 07611819378902, 07611819459915, 07611819358669, 07611819365711, 07611819366879, 07611819345973, 07611819479371, 07611819494923, 07611819370777, 07611819417779, 07611819347960, 07611819347731, 07611819344853, 07611819345287, 07611819347748, 07611819522657, 07611819365384, 07611819343320, 07611819459991, 07611819365858, 07611819370753, 07611819479623, 07611819418219, 07611819358614, 07611819365605, 07611819345980, 07611819343740, 07611819470828, 07611819425491, 07611819418066, 07611819347700, 07611819417939, 07611819460164, 07611819344945, 07611819418240, 07611819479456, 07611819365865, 07611819370623, 07611819365827, 07611819343603, 07611819343399, 07611819522756
Basic UDI-DI
7611819a00441JJ, 7611819a00266JQ, 7611819a00404JC, 7611819a00070J5, 7611819a00392JW, 7611819a00401J6, 7611819a00403JA
EMDN code
P09070304, P09070302, Z12139099
Device class
Class IIb
Class IIa
EU registration type
Standard device
EU market of registration
Belgium

Manufacturer details

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

Related devices

Category: Bone-screw internal spinal fixation system connector

Other devices from Synthes GmbH

See all devices from Synthes GmbH →

Properties

  • Supplied sterile NoEUDAMEDYesEUDAMED
  • Sterilise before use YesEUDAMEDNoEUDAMED
  • Implantable YesEUDAMEDNoEUDAMED
  • Sutures
  • Contains CMR substances (carcinogenic, mutagenic or toxic to reproduction) NoEUDAMEDYesEUDAMED

Other properties (10)

  • Reusable: No
  • Contains latex: No
  • Reprocessed single-use device: No
  • Incorporates a substance derived from human blood or plasma: No
  • Contains human tissues or cells: No
  • Contains animal tissues or cells: No
  • Contains endocrine-disrupting substances: No
  • Administering medicine: No
  • Measuring function: No
  • Incorporates a medicinal substance: No