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Terumo

by Terumo Penpol Private Limited EUDAMED

Active European Union

Ref PB-3AG456M8Y

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-58904009332865 Basic UDI-DIDate28 May 2026RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Expiring

Certificates: none listed in EUDAMED

Specification

EUDAMED

Device Name
Terumo Blood Bag
Model / Reference
PB-3AG456M8Y
Primary DI / UDI-DI
58904009332865
Basic UDI-DI
B-58904009332865
EMDN Code
B0101020201 Donor blood collection triple bags, w/o filters and kit
Device Class
Class III
Market of Registration
Belgium

Manufacturer details

EUDAMED SRN
IN-MF-000001071
Authorised representative
Terumo BCT Europe N.V. BE-AR-000001030

Other devices from Terumo Penpol Private Limited

See all devices from Terumo Penpol Private Limited →

Properties

Show properties
  • Sterile
  • Incorporates Medicinal Product
Other properties (9)
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No