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Materialise Titanium 3D Printed Guides

by Materialise NV 56 variants

Ref CMF.Ti053D

Materialise Titanium 3D Printed Guides (CMF.Ti053D) is a Class IIa device made by Materialise NV, registered in EUDAMED on 16 Jul 2026 (Basic UDI-DI 54200603B0053T9), 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 Number54200603B0053T9 Basic UDI-DI 05420060344244UDI-DIDate16 Jul 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Model / reference
CMF.Ti053D
Primary DI / UDI-DI
05420060344244
Basic UDI-DI
54200603B0053T9
EMDN code
P091399 Orthopaedic implant instruments, single-use - other
Device class
Class IIa
EU registration type
Standard device
EU market of registration
France

Manufacturer details

EUDAMED SRN
BE-MF-000000034

Similar devices in this category

Other devices filed under ORTHOPAEDIC IMPLANT INSTRUMENTS, SINGLE-USE - OTHER.

Other devices from Materialise NV

See all devices from Materialise NV →

Properties

  • Sterilise before use
Other properties (13, all answered No)