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BD BodyGuard™

by Caesarea Medical Electronics Ltd. 12 variants

Ref 190-900PXCVI

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number0885403MAULRMBZ9J Basic UDI-DI 00885403449515UDI-DIDate7 May 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
BD BodyGuard™ Lockboxes
Model / Reference
190-900PXCVI
Primary DI / UDI-DI
00885403449515
Basic UDI-DI
0885403MAULRMBZ9J
EMDN Code
Z12030380 Infusion instruments - hardware accessories
Device Class
Class I
EU market of registration
Belgium

Manufacturer details

EUDAMED SRN
IL-MF-000030321
Authorised representative
Becton Dickinson Ireland Limited IE-AR-000007610

Other devices from Caesarea Medical Electronics Ltd.

See all devices from Caesarea Medical Electronics Ltd. →

Properties

Other properties (13)

  • Sterile: No
  • 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