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D-Reamer

by QuantièmePlus SA 31 variants

Ref RM21

Active European Union

CE MDR

Valid until

Not listed

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

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number764016863REUTJS Basic UDI-DI 07640168630218UDI-DIDate22 Dec 2022RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
D-Reamer
Model / Reference
RM21
Primary DI / UDI-DI
07640168630218
Basic UDI-DI
764016863REUTJS
EMDN Code
L091102 Orthopaedic prostheses reamers and burs, reusable
Device Class
Class IIa
EU market of registration
France

Manufacturer details

EUDAMED SRN
CH-MF-000011186
Authorised representative
LAPE Médical FR-AR-000007694

Related devices

Category: Acetabular orthopaedic reamer

Other devices from QuantièmePlus SA

See all devices from QuantièmePlus SA →

Properties

  • Reusable

Other properties (12)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No