← Back to catalogue

Cervios

EUDAMED

Class IIa (EU MDR)

Ref 396.936Model Spine Trial Implants for Cervios

by Synthes GmbH

Identity

Trade Name
CERVIOS EUDAMED
Device Name
Cervios Trial Implant Wedge-Shaped Curved EUDAMED
Model / Reference
Spine Trial Implants for Cervios EUDAMED
396.936 EUDAMED

Identifiers

Primary DI / UDI-DI
07611819738744 EUDAMED
Basic UDI-DI
7611819a00518JU 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

Cervios 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

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

Sources (1)

  • EUDAMED 6c61881a-a61c-47a3-8776-ef55c35dfe52 61 fields · synced Jun 19, 2026