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Targon Pft

EUDAMED

Class I (EU MDR)

Ref KH512R

by Aesculap AG

Identity

Trade Name
TARGON PFT EUDAMED
Device Name
TARGON_PF-PFT-FN tray EUDAMED
Model / Reference
KH512R EUDAMED

Identifiers

Primary DI / UDI-DI
04046963416737 EUDAMED
Basic UDI-DI
40392390000010692A EUDAMED
Direct Marketing DI
04046963416737 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

Targon Pft 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 3149afe0-6231-46ff-a27b-4d3c0fb39b73 61 fields · synced Jun 18, 2026