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MatrixMIDFACE

EUDAMED

Class IIa (EU MDR)

Ref 03.503.365Model Craniomaxillofacial Bending Templates and Sizers

by Synthes GmbH

Identity

Trade Name
MatrixMIDFACE EUDAMED
Device Name
Craniomaxillofacial Bending Templates and Sizers EUDAMED
Model / Reference
Craniomaxillofacial Bending Templates and Sizers EUDAMED
03.503.365 EUDAMED

Identifiers

Primary DI / UDI-DI
07611819351073 EUDAMED
Basic UDI-DI
7611819a00070J5 EUDAMED
Direct Marketing DI
07611819351073 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

MatrixMIDFACE 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 a6e459d2-c0b3-4d42-9304-2e4b1f2fe60c 61 fields · synced Jun 19, 2026