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Reveos NLR

by Terumo BCT, Ltd. XI EUDAMED

Ref 5NG456S0YModel Reveos NLR

EMDN B0101020102

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-05054638301119 Basic UDI-DIDate25 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 NLR, 5NG456S0Y
Primary DI / UDI-DI
05054638301119
Basic UDI-DI
B-05054638301119
EMDN Code
B0101020102 Donor blood collection quintuple 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 05054638301119|B-05054638301119 61 fields · synced 24 Oct 2026