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Reamer

by FX Shoulder Solutions

Part of a family of 12 devices: see the family page

Ref 903-0078

Reamer (903-0078) is a Class I device made by FX Shoulder Solutions, registered in EUDAMED on 23 Jun 2026 (Basic UDI-DI 37010373REAMERAM), 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 Number37010373REAMERAM Basic UDI-DI 03701037315460UDI-DIDate23 Jun 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device name
Reamer
Model / reference
903-0078
Primary DI / UDI-DI
03701037315460
Basic UDI-DI
37010373REAMERAM
Direct marketing DI
03701037315460
EMDN code
L091102 Orthopaedic prostheses reamers and burs, reusable
Device class
Class I
EU registration type
Standard device
EU market of registration
France

Manufacturer details

EUDAMED SRN
FR-MF-000000465

Similar devices in this category

Other devices filed under ORTHOPAEDIC PROSTHESES REAMERS AND BURS, REUSABLE.

Other devices from FX Shoulder Solutions

See all devices from FX Shoulder Solutions →

Properties

  • Sterilise before use
  • Reusable
Other properties (12, all answered No)