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Targon

EUDAMED

Class I (EU MDR)

Ref KH460R

by Aesculap AG

Identity

Trade Name
TARGON EUDAMED
Device Name
TARGON_F-T-RF-TX instrument I EUDAMED
Model / Reference
KH460R EUDAMED

Identifiers

Primary DI / UDI-DI
04046963360597 EUDAMED
Basic UDI-DI
4039239000001073ZW EUDAMED
EMDN Code
L0903 ORTHOPAEDIC SURGERY HAMMERS, REUSABLE EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany 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

Targon by Aesculap AG — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Aesculap AG
EUDAMED SRN
DE-MF-000005504

Sources (1)

  • EUDAMED dc9703fa-9a68-427d-aef4-9dff7bc8c635 61 fields · synced Jun 18, 2026