Skip to content

Matrix Spine Instruments for Insertion and Extraction

by Synthes GmbH 38 variants

Ref 03.632.036, 03.632.400, 03.632.005, 03.632.060, 03.632.080, 03.616.081, 03.616.037, 03.632.010, 03.632.099, 03.616.038, 03.632.038, 03.616.048, 03.616.035, 03.632.029, 03.632.169, 03.632.026, 03.616.052, 03.616.070, 03.632.053, 03.632.002, 03.632.204, 03.616.050, 03.632.401, 03.616.063, 03.632.058, 03.632.003, 03.616.040, 03.637.001, 03.620.091, 03.632.050, 03.632.004, 03.632.012, 03.616.036, 03.632.090, 03.632.074Model Matrix Spine Instruments for Insertion and Extraction

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 Number7611819a00126J7 Basic UDI-DI Date14 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  • Withdrawn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
Matrix Spine Instruments for Insertion and Extraction
Model / Reference
Matrix Spine Instruments for Insertion and Extraction, 03.632.036, 03.632.400, 03.632.005, 03.632.060, 03.632.080, 03.616.081, 03.616.037, 03.632.010, 03.632.099, 03.616.038, 03.632.038, 03.616.048, 03.616.035, 03.632.029, 03.632.169, 03.632.026, 03.616.052, 03.616.070, 03.632.053, 03.632.002, 03.632.204, 03.616.050, 03.632.401, 03.616.063, 03.632.058, 03.632.003, 03.616.040, 03.637.001, 03.620.091, 03.632.050, 03.632.004, 03.632.012, 03.616.036, 03.632.090, 03.632.074
Primary DI / UDI-DI
07611819379435, 07611819502024, 07611819378087, 07611819379596, 07611819377325, 07611819498730, 07611819416840, 07611819379237, 07611819388086, 07611819416857, 07611819379459, 07611819417458, 07611819416826, 07611819379398, 07611819377462, 07611819391475, 07611819417489, 07611819417663, 07611819379558, 07611819378063, 07611819377479, 07611819417465, 07611819502031, 07611819417595, 07611819379589, 07611819391468, 07611819416871, 07611819433830, 07611819359505, 07611819379534, 07611819378070, 07611819379251, 07611819416833, 07611819377349, 07611819377301
Basic UDI-DI
7611819a00126J7
Direct Marketing DI
07611819379435
07611819502024
07611819378087
07611819379596
07611819377325
07611819498730
07611819416840
07611819379237
07611819388086
07611819416857
07611819379459
07611819417458
07611819416826
07611819379398
07611819377462
07611819391475
07611819417489
07611819417663
07611819379558
07611819378063
07611819377479
07611819417465
07611819502031
07611819417595
07611819379589
07611819391468
07611819416871
07611819433830
07611819359505
07611819379534
07611819378070
07611819379251
07611819416833
07611819377349
07611819377301
EMDN Code
L091001 Instruments for insertion and extraction of materials for osteosynthesis, reusable
Device Class
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

  • Reusable
  • CMR Substance YesEUDAMEDNoEUDAMED

Other properties (11)

  • Sterile: No
  • Implantable: 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