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Targon Fn

by Aesculap AG 8 variants

Ref KO824T

Active European Union

CE MDD

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-04046963090869 Basic UDI-DI 04046963090869UDI-DIDate16 Oct 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDD Active

EU market availability

Made available in 27 countries, as listed in EUDAMED:

Declared by the manufacturer in EUDAMED for this device version; may not cover every market.

  • Austria since 24 Apr 2006
  • Belgium since 24 Apr 2006
  • Bulgaria since 24 Apr 2006
  • Croatia since 24 Apr 2006
  • Cyprus since 24 Apr 2006
  • Czechia since 24 Apr 2006
  • Denmark since 24 Apr 2006
  • Estonia since 24 Apr 2006
  • Finland since 24 Apr 2006
  • France since 24 Apr 2006
  • Germany since 24 Apr 2006
  • Greece since 24 Apr 2006
  • Hungary since 24 Apr 2006
  • Ireland since 24 Apr 2006
  • Italy since 24 Apr 2006
  • Latvia since 24 Apr 2006
  • Lithuania since 24 Apr 2006
  • Luxembourg since 24 Apr 2006
  • Malta since 24 Apr 2006
  • Netherlands since 24 Apr 2006
  • Poland since 24 Apr 2006
  • Portugal since 24 Apr 2006
  • Romania since 24 Apr 2006
  • Slovakia since 24 Apr 2006
  • Slovenia since 24 Apr 2006
  • Spain since 24 Apr 2006
  • Sweden since 24 Apr 2006

Last checked 23 Oct 2026.

Specification

EUDAMED

Device Name
Targon Fn Telescrew 90+10MM
Model / Reference
KO824T
Primary DI / UDI-DI
04046963090869
Basic UDI-DI
B-04046963090869
EMDN Code
P09120503 Osteosynthesis screw-plate systems
Device Class
Class IIb
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000005504

Other devices from Aesculap AG

See all devices from Aesculap AG →

Properties

  • Sterile
  • Implantable

Other properties (11)

  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No