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Duoflex+ 180

by Meditech International Inc Canada EUDAMED

Ref +B271LSB48900Model LS-B 4890 EMDN Z120614

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-+B271LSB48900 Basic UDI-DIDate12 Jun 2024RegisteredStatusWithdrawn No longer placed on the EU market

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDD Withdrawn

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 24 Oct 2026

Model / Reference
LS-B 4890, +B271LSB48900
Primary DI / UDI-DI
+B271LSB48900
Basic UDI-DI
B-+B271LSB48900
EMDN Code
Z120614 Infrared ultraviolet ray lamps
Device Class
Class IIa
Market of Registration
Northern Ireland

Manufacturer details

EUDAMED SRN
CA-MF-000011432
Authorised representative
Obelis s.a. BE-AR-000000106

Other devices from Meditech International Inc

Properties & raw data

Show properties, registry sources and raw records
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

Sources (1)

  • EUDAMED 33679948-6a6b-4aa3-94f2-b47940e211cf 61 fields · synced 24 Oct 2026