Skip to content

Reveos LR

by Terumo BCT, Ltd. XI EUDAMED

Ref 4FG456S0Model Reveos LR

EMDN B0101020101

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-05054638300853 Basic UDI-DIDate9 Sep 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Expiring (legacy directive)
  • Not covered

European Union — CE/MDD Expiring (legacy directive)

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 24 Oct 2026

Model / Reference
Reveos LR, 4FG456S0
Primary DI / UDI-DI
05054638300853
Basic UDI-DI
B-05054638300853
EMDN Code
B0101020101 Donor blood collection quadruple bags, with filters and kits
Device Class
Class IIb
Market of Registration
Belgium

Manufacturer details

EUDAMED SRN
XI-MF-000004232

Other devices from Terumo BCT, Ltd.

Properties & raw data

Show properties, registry sources and raw records
  • Sterile
  • Animal Tissues
  • Incorporates Medicinal Product
Other properties (8)
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Administering Medicine: No
  • Measuring Function: No

Sources (1)

  • EUDAMED fe3f4ac7-2d32-4a08-84f5-d466aecf13be 61 fields · synced 24 Oct 2026