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Trj

by Aesculap AG 17 variants

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

Ref NT130R

Trj (NT130R) is a Class I device made by Aesculap AG, registered in EUDAMED on 8 Oct 2025 (Basic UDI-DI 4039239000000415ZV), active as of 25 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 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number4039239000000415ZV Basic UDI-DI 04046963643454UDI-DIDate8 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  • Withdrawn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
Model / reference
NT130R
Primary DI / UDI-DI
04046963643454
Basic UDI-DI
4039239000000415ZV
Direct marketing DI
04046963643454
EMDN code
L091199 Orthopaedic prosthetics instruments, reusable - other
Device class
Class I
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
Other properties (12, all answered No)