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MatrixMIDFACE

EUDAMED

Class IIb (EU MDR)

Ref 04.503.955.04CModel MatrixMIDFACE Screws

by Synthes GmbH

Identity

Trade Name
MatrixMIDFACE EUDAMED
Device Name
MatrixMIDFACE Screws EUDAMED
Model / Reference
MatrixMIDFACE Screws EUDAMED
04.503.955.04C EUDAMED

Identifiers

Primary DI / UDI-DI
07612334183699 EUDAMED
Basic UDI-DI
7611819a00553JW EUDAMED
Unit of Use DI
87612334183695 EUDAMED
EMDN Code
P09120601 CORTICAL SCREWS EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
Belgium EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

Yes

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Sutures

Yes

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 bone screw (non-sliding)

MatrixMIDFACE by Synthes GmbH — Class IIb — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic bone screw (non-sliding).

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 4279bf8e-3c8d-489e-883a-977be096a1c3 61 fields · synced Jun 17, 2026