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Trj

by Aesculap AG 17 variants

Part of a family of 15 devices: see the family pagePart of a family of 15 devices: see the family page

Ref NT125R, NT112, NT117R, NT167R, NT159R, NT124R, NT157R, NT121R, NT123R, NT129R, ND478R, NT171R, NT127R, NT136R, NT115R, NT169R, NT131R, NT162R, NT110, NT139R, NT168R

Trj (NT125R) is a device classified as Class I and Class IIa in the EU made by Aesculap AG, registered in EUDAMED on 8 Oct 2025 (Basic UDI-DI 4039239000000415ZV), active as of 22 Oct 2026.

Active European Union

CE MDR

Valid until

No date given

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

Source EUDAMED, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number4039239000000415ZV Basic UDI-DI Date8 Oct 2025RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device name
TRJ preparation instrument
TRJ instrument set
THA adapter, handle, gauge
TRJ insertion instrument
TRJ instrument
Model / reference
NT125R, NT112, NT117R, NT167R, NT159R, NT124R, NT157R, NT121R, NT123R, NT129R, ND478R, NT171R, NT127R, NT136R, NT115R, NT169R, NT131R, NT162R, NT110, NT139R, NT168R
Primary DI / UDI-DI
04046963643409, 04046963643874, 04046963643348, 04046963893781, 04046963893712, 04046963643393, 04046963891961, 04046963643362, 04046963643386, 04046963643447, 04046963653781, 04046963893859, 04046963643423, 04046963643485, 04046963643324, 04046963893828, 04046963643461, 04046963893736, 04046963643867, 04046963643508, 04046963893811
Basic UDI-DI
4039239000000415ZV, 40392390000027512Z, 403923900000195134, 403923900000275233, 40392390000027502X
Direct marketing DI
04046963643409
04046963643348
04046963893781
04046963893712
04046963643393
04046963891961
04046963643362
04046963643386
04046963643447
04046963653781
04046963893859
04046963643423
04046963643485
04046963643324
04046963893828
04046963643461
04046963893736
04046963643508
04046963893811
EMDN code
L091199 Orthopaedic prosthetics instruments, reusable - other
Device class
Class I
Class IIa
EU registration type
Standard device
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000005504

Similar devices in this category

Other devices filed under ORTHOPAEDIC PROSTHETICS INSTRUMENTS, REUSABLE - OTHER.

Other devices from Aesculap AG

See all devices from Aesculap AG →

Properties

  • Sterilise before use
  • Reusable YesEUDAMEDNoEUDAMED
  • Contains CMR substances (carcinogenic, mutagenic or toxic to reproduction) NoEUDAMEDYesEUDAMED
Other properties (11, all answered No)