Skip to content

Orthopaedic Sizing Templates

by Synthes GmbH 39 variants

Ref 03.100.035, 03.100.034, 03.100.061, 03.132.268, 03.221.101, 03.164.006, 03.132.258, 329.660, 03.132.360, 03.132.161, 03.100.060, 03.132.154, 03.100.342, 03.164.002, 03.100.348, 03.132.263, 03.132.367, 03.132.261, 03.132.159, 329.608, 03.132.260, 03.100.050, 03.221.092, 03.221.151, 03.132.354, 03.100.358, 03.132.152, 03.221.155, 329.607, 03.221.153, 03.100.070, 03.100.352, 03.221.152, 03.132.256, 03.132.259Model Orthopaedic Sizing Templates

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 Number7611819a00065JC 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  • Withdrawn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

Device Name
Orthopaedic Sizing Templates
Model / Reference
Orthopaedic Sizing Templates, 03.100.035, 03.100.034, 03.100.061, 03.132.268, 03.221.101, 03.164.006, 03.132.258, 329.660, 03.132.360, 03.132.161, 03.100.060, 03.132.154, 03.100.342, 03.164.002, 03.100.348, 03.132.263, 03.132.367, 03.132.261, 03.132.159, 329.608, 03.132.260, 03.100.050, 03.221.092, 03.221.151, 03.132.354, 03.100.358, 03.132.152, 03.221.155, 329.607, 03.221.153, 03.100.070, 03.100.352, 03.221.152, 03.132.256, 03.132.259
Primary DI / UDI-DI
07611819796782, 07611819796775, 07611819796867, 07611819687363, 07612334219084, 07612334216595, 07611819683082, 07611819021433, 07611819690400, 07611819687455, 07611819796850, 07611819687400, 07611819483408, 07612334216557, 07611819483439, 07611819687325, 07611819690424, 07611819687318, 07611819687448, 07611819737082, 07611819683105, 07611819796836, 07612334219039, 07612334219121, 07611819690394, 07611819483484, 07611819687387, 07612334150936, 07611819723054, 07612334219145, 07611819796874, 07611819483453, 07612334219138, 07611819683068, 07611819683099
Basic UDI-DI
7611819a00065JC
Direct Marketing DI
07611819796782
07611819796775
07612334219084
07612334216595
07611819683082
07611819021433
07611819690400
07611819483408
07612334216557
07611819483439
07611819737082
07611819683105
07612334219039
07612334219121
07611819483484
07612334150936
07611819723054
07612334219145
07611819483453
07612334219138
07611819683099
EMDN Code
Z12139099 Various orthopaedic and traumatology instruments - other
Device Class
Class IIa
EU market of registration
Belgium

Manufacturer details

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

Related devices

Category: Orthopaedic guidewire, reusable

Other devices from Synthes GmbH

See all devices from Synthes GmbH →

Properties

  • CMR Substance NoEUDAMEDYesEUDAMED

Other properties (12)

  • Sterile: No
  • Implantable: No
  • Reusable: 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