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Craniomaxillofacial Cutting Instruments

EUDAMED

Class I (EU MDR)

Ref 311.230Model Craniomaxillofacial Cutting Instruments

by Synthes GmbH

Identity

Device Name
Craniomaxillofacial Cutting Instruments EUDAMED
Model / Reference
Craniomaxillofacial Cutting Instruments EUDAMED
311.230 EUDAMED

Identifiers

Primary DI / UDI-DI
07611819019270 EUDAMED
Basic UDI-DI
7611819a00108J5 EUDAMED
Direct Marketing DI
07611819019270 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

Craniomaxillofacial Cutting Instruments 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 c4642efb-3fff-4ddd-ba1b-b96002fe68d7 61 fields · synced Jun 18, 2026