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Leaseir MHR Laser System

by Leaseir Technologies, S.L.U.

Ref Leaseir MHR Laser SystemModel MHR 230

Active European Union

CE MDD

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/MDD NumberB-MHR-Laser-System-U7 Basic UDI-DI D-MHR-Laser-System-U7UDI-DIDate18 Jul 2023RegisteredStatusActive

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  • Withdrawn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/MDD Active

Specification

EUDAMED

Device Name
Leaseir MHR Laser System
Model / Reference
MHR 230, Leaseir MHR Laser System
Primary DI / UDI-DI
D-MHR-Laser-System-U7
Basic UDI-DI
B-MHR-Laser-System-U7
EMDN Code
Z12011016 Diode surgical laser
Device Class
Class IIb
EU market of registration
France

Manufacturer details

EUDAMED SRN
ES-MF-000002995

Other devices from Leaseir Technologies, S.L.U.

Properties

Other properties (11)

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