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Awl

EUDAMED

Class I (EU MDR)

Ref 03.647.990Model Zero P Instruments Orthopaedic Surgery Cutting Instruments

by Synthes GmbH

Identity

Device Name
Awl EUDAMED
Model / Reference
Zero P Instruments Orthopaedic Surgery Cutting Instruments EUDAMED
03.647.990 EUDAMED

Identifiers

Primary DI / UDI-DI
07611819498099 EUDAMED
Basic UDI-DI
7611819a00171JC EUDAMED
Direct Marketing DI
07611819498099 EUDAMED
EMDN Code
L090999 ORTHOPAEDIC SURGERY CUTTING INSTRUMENTS, REUSABLE - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Belgium EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

Yes

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: Bone cutting forceps, reusable

Awl by Synthes GmbH — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Bone cutting forceps, 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 210e6c5b-c3fb-4634-a364-2d63a594bf87 61 fields · synced Jun 20, 2026