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Xrl

EUDAMED

Class IIa (EU MDR)

Ref 03.807.513Model Spine Trial Implants for XRL Medium

by Synthes GmbH

Identity

Trade Name
XRL EUDAMED
Device Name
XRL Medium Endplate Trial Trial Implant Integrated Central Body Endplate EUDAMED
Model / Reference
Spine Trial Implants for XRL Medium EUDAMED
03.807.513 EUDAMED

Identifiers

Primary DI / UDI-DI
07611819406544 EUDAMED
Basic UDI-DI
7611819a00527JV EUDAMED
Direct Marketing DI
07611819406544 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

Xrl 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 d48185a4-079c-4f29-8935-e09a02e946ce 61 fields · synced Jun 18, 2026