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Ambu® aBox 2

by Ambu A/S Denmark EUDAMED

Ref 505001000EUC2Model Ambu aBox 2 EMDN Z12020406

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number570748030100700107U Basic UDI-DIDate18 Jun 2026RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 22 Oct 2026

Device Name
Ambu aBox 2
Model / Reference
Ambu aBox 2, 505001000EUC2
Primary DI / UDI-DI
05707480156238
Basic UDI-DI
570748030100700107U
Direct Marketing DI
05707480146710
EMDN Code
Z12020406 Video processors
Device Class
Class IIa
Special Device Type
Software
Market of Registration
Greece

Manufacturer details

EUDAMED SRN
DK-MF-000001437

Other devices from Ambu A/S

See all devices from Ambu A/S →

Properties & raw data

Show properties, registry sources and raw records
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

Sources (1)

  • EUDAMED 6d722269-e357-4dae-aca4-b90e2c5684e9 61 fields · synced 22 Oct 2026