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BD Alaris™

by BD Switzerland Sarl Switzerland EUDAMED

Ref 500-002V

EMDN A03020199

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-0761320302800LFB Basic UDI-DIDate20 Oct 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

Device Name
Tiva 2 Way Set. Anti-Siphon Valve. Back Check Valve.
Model / Reference
500-002V
Primary DI / UDI-DI
D-0761320302800LFB
Basic UDI-DI
B-0761320302800LFB
EMDN Code
A03020199 Extensions - other
Device Class
Class IIa
Market of Registration
Belgium

Manufacturer details

EUDAMED SRN
CH-MF-000026539
Authorised representative
Becton Dickinson Ireland Limited IE-AR-000007610

Other devices from Bd Switzerland SARL

See all devices from Bd Switzerland SARL →

Properties & raw data

Show properties, registry sources and raw records
  • Sterile
  • Administering Medicine
Other properties (11)
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No

Sources (1)

  • EUDAMED D-0761320302800LFB|B-0761320302800LFB 61 fields · synced 24 Oct 2026