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BD Q-Syte™

by Becton Dickinson Infusion Therapy Systems Inc. 19 variants

Ref 385108

Active European Union

CE MDD

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-0038290385108LHA Basic UDI-DI D-0038290385108LHAUDI-DIDate20 Oct 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDD Active

Specification

EUDAMED

Device Name
BD Q-Syte™ Vial Access Adapter
Model / Reference
385108
Primary DI / UDI-DI
D-0038290385108LHA
Basic UDI-DI
B-0038290385108LHA
EMDN Code
A070103 Infusion tubing adapters and connectors
Device Class
Class IIa
EU market of registration
Belgium

Manufacturer details

EUDAMED SRN
US-MF-000017719
Authorised representative
Becton Dickinson Distribution Center NV BE-AR-000014947

Other devices from Becton Dickinson Infusion Therapy Systems Inc.

See all devices from Becton Dickinson Infusion Therapy Systems Inc. →

Properties

  • Sterile

Other properties (12)

  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No