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Targon Rf

EUDAMED

Class I (EU MDR)

Ref KH335R

by Aesculap AG

Identity

Trade Name
TARGON RF EUDAMED
Device Name
TARGON_F-T-RF-TX tray EUDAMED
Model / Reference
KH335R EUDAMED

Identifiers

Primary DI / UDI-DI
04038653257218 EUDAMED
Basic UDI-DI
40392390000017012B EUDAMED
Direct Marketing DI
04038653257218 EUDAMED
EMDN Code
S010401 TRAYS, BASKETS, TUBS FOR STERILISATION AND THEIR COMPONENTS 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

Category: Instrument tray, reusable

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

Similar devices

Also classified as Instrument tray, 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 9805a18e-fa0e-4ce2-aaa4-1f453592f31a 61 fields · synced May 22, 2026