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Orthopaedic Reduction Instruments

by Synthes GmbH 17 variants

Ref 03.211.463, 352.055, 03.164.012, 03.211.468, 359.210, 392.966, 03.010.369, 03.507.004, 03.118.008, 324.024, 03.430.015, 325.030, 03.118.005, 398.540, 324.033, 03.211.464, 03.100.019, 395.450, 321.120, 03.118.006, 328.020, 394.460, 03.100.018, 03.430.017, 359.207, 03.043.023Model Orthopaedic Reduction Instruments

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number7611819a00049JE Basic UDI-DI Date3 Dec 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  • Withdrawn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
Orthopaedic Reduction Instruments
Model / Reference
Orthopaedic Reduction Instruments, 03.211.463, 352.055, 03.164.012, 03.211.468, 359.210, 392.966, 03.010.369, 03.507.004, 03.118.008, 324.024, 03.430.015, 325.030, 03.118.005, 398.540, 324.033, 03.211.464, 03.100.019, 395.450, 321.120, 03.118.006, 328.020, 394.460, 03.100.018, 03.430.017, 359.207, 03.043.023
Primary DI / UDI-DI
07611819614871, 07611819259829, 07612334216656, 07611819639287, 07611819713468, 07611819759312, 07611819326965, 07611819377820, 07611819503595, 07611819895614, 07612334236449, 07611819155244, 07611819503564, 07611819027145, 07611819221345, 07611819614888, 07611819796638, 07611819203310, 07611819021051, 07611819503571, 07611819155275, 07611819025769, 07611819796621, 07612334236463, 07611819710580, 07612334171047
Basic UDI-DI
7611819a00049JE
Direct Marketing DI
07611819614871
07611819259829
07612334216656
07611819639287
07611819713468
07611819759312
07611819326965
07611819377820
07611819503595
07612334236449
07611819155244
07611819503564
07611819027145
07611819221345
07611819614888
07611819796638
07611819203310
07611819021051
07611819503571
07611819155275
07611819025769
07611819796621
07612334236463
07611819710580
07612334171047
EMDN Code
L091001, L0999, P0912040102, L091099, L091301, L0902
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 NoEUDAMEDYesEUDAMED

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