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Antiplatelet Reagent

by Haemonetics S.A. EUDAMED

Active European Union

Ref 07-670

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number081274701REAG00143 Basic UDI-DIDate11 Sep 2026RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/IVDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED

Model / Reference
07-670
Primary DI / UDI-DI
90812747018605
Basic UDI-DI
081274701REAG00143
Unit of Use DI
00812747018602
EMDN Code
W01030299 Haemostasis reagents - other
Device Class
Class A
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
CH-MF-000034549
Authorised representative
Haemonetics Italia s.r.l IT-AR-000021067

Other devices from Haemonetics S.A.

See all devices from Haemonetics S.A. →

Properties

  • Animal Tissues
  • Reagent
  • Near-Patient Testing
  • Professional Testing
  • New Device

Other properties (6)

  • Sterile: No
  • Human Tissues: No
  • Microbial Substances: No
  • Self Testing: No
  • Companion Diagnostics: No
  • Surgical Instrument: No