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Trilliance

by Aesculap AG 2 variants

Part of a family of 68 devices: see the family page

Ref ND391R

Trilliance (ND391R) is a Class I device made by Aesculap AG, registered in EUDAMED on 8 Oct 2025 (Basic UDI-DI 40392390000004542A), active as of 24 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 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number40392390000004542A Basic UDI-DI 04038653274383UDI-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  • Withdrawn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
BICONTACT instrument Ir
Model / reference
ND391R
Primary DI / UDI-DI
04038653274383
Basic UDI-DI
40392390000004542A
Direct marketing DI
04038653274383
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)