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SYNFIX Evolution

EUDAMED

Class IIa (EU MDR)

Ref 03.835.124Model Spine Trial Implants for SYNFIX Evolution

by Synthes GmbH

Identity

Trade Name
SYNFIX Evolution EUDAMED
Device Name
SYNFIX Evolution Footprint Trial Trial Implant Small Medium Large EUDAMED
Model / Reference
Spine Trial Implants for SYNFIX Evolution EUDAMED
03.835.124 EUDAMED

Identifiers

Primary DI / UDI-DI
07611819680548 EUDAMED
Basic UDI-DI
7611819a00524JP EUDAMED
Direct Marketing DI
07611819680548 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

SYNFIX Evolution 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 fc828b79-187a-458d-9341-9f8d6b745378 61 fields · synced May 23, 2026