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Zero-P

EUDAMED

Class IIa (EU MDR)

Ref 03.617.726Model Spine Trial Implants for Zero-P

by Synthes GmbH

Identity

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

Identifiers

Primary DI / UDI-DI
07611819932715 EUDAMED
Basic UDI-DI
7611819a00528JX EUDAMED
Direct Marketing DI
07611819932715 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 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 db1891f5-eca7-4262-a9c6-d9d8cb48647b 61 fields · synced May 23, 2026