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Dhs

EUDAMED

Class IIa (EU MDR)

Ref 338.650Model Orthopaedic Sizing Templates

by Synthes GmbH

Identity

Trade Name
DHS EUDAMED
Device Name
Orthopaedic Sizing Templates EUDAMED
Model / Reference
Orthopaedic Sizing Templates EUDAMED
338.650 EUDAMED

Identifiers

Primary DI / UDI-DI
07611819056695 EUDAMED
Basic UDI-DI
7611819a00065JC EUDAMED
Direct Marketing DI
07611819056695 EUDAMED
EMDN Code
Z12139099 VARIOUS ORTHOPAEDIC AND TRAUMATOLOGY INSTRUMENTS - OTHER EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Belgium EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Category: Orthopaedic guidewire, reusable

Dhs by Synthes GmbH — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic guidewire, reusable.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Synthes GmbH
EUDAMED SRN
CH-MF-000013345
Authorised Representative
DePuy Ireland UC IE-AR-000009328

Sources (1)

  • EUDAMED 65cc3af9-57e8-42bd-bafa-65ac01bef7f6 61 fields · synced Jun 19, 2026