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6-Drawer Medicine Cart

by inspital medical technology GmbH

Ref AB20.60Model AB10.60, AB11.60, AB12.60, AB10.50, AB10.66, AB30.00, AB30.01, AB20.60, AB20.90, AB40.32, AB40.40, AB41.32, AB10.10, AB10.20

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number42519311AB20GMBHVF Basic UDI-DI 04251931107498UDI-DIDate21 Jul 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  • Withdrawn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
Emergency Cart
Model / Reference
AB10.60, AB11.60, AB12.60, AB10.50, AB10.66, AB30.00, AB30.01, AB20.60, AB20.90, AB40.32, AB40.40, AB41.32, AB10.10, AB10.20
Primary DI / UDI-DI
04251931107498
Basic UDI-DI
42519311AB20GMBHVF
EMDN Code
V0899 Medical support equipment - other
Device Class
Class I
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000013966

Other devices from inspital medical technology GmbH

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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