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Targon Pft

EUDAMED

Class I (EU MDR)

Ref KH549R

by Aesculap AG

Identity

Trade Name
TARGON PFT EUDAMED
Device Name
TARGON_PF-PFT-FN instrument Ir EUDAMED
Model / Reference
KH549R EUDAMED

Identifiers

Primary DI / UDI-DI
04046963383985 EUDAMED
Basic UDI-DI
4039239000001070ZQ EUDAMED
EMDN Code
L091099 OSTEOSYNTHESIS INSTRUMENTS, REUSABLE - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

Yes

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

Category: Surgical implant template, reusable

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

Similar devices

Also classified as Surgical implant template, reusable.

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 2d370b50-80f3-496c-82d0-d0e06ed3f194 61 fields · synced Oct 8, 2026