← Back to catalogue

Zero-P Va

EUDAMED

Class IIa (EU MDR)

Ref 03.647.750Model Spine Trial Implants for Zero-P VA

by Synthes GmbH

Identity

Trade Name
ZERO-P VA EUDAMED
Device Name
Zero-P VA Trial Spacer Lordotic Convex Large EUDAMED
Model / Reference
Spine Trial Implants for Zero-P VA EUDAMED
03.647.750 EUDAMED

Identifiers

Primary DI / UDI-DI
07611819404175 EUDAMED
Basic UDI-DI
7611819a00529JZ EUDAMED
Direct Marketing DI
07611819404175 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

Yes

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

Zero-P Va 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 5cd18239-4065-4315-82a4-78a4821c2fa0 61 fields · synced May 23, 2026