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myAbbVieCare Android

by AbbVie Inc.

Ref 0AV103

myAbbVieCare Android (0AV103) is a Class I device made by Abbvie Inc., registered in EUDAMED on 21 Sep 2026 (Basic UDI-DI 8054083000V0AV103WN), active as of 24 Oct 2026.

Active European Union

CE MDR

Valid until

No date given

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

Source EUDAMED, synced 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number8054083000V0AV103WN Basic UDI-DI 08054083028163UDI-DIDate21 Sep 2026RegisteredStatusActive

Official records

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  • Withdrawn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

Model / reference
0AV103
Primary DI / UDI-DI
08054083028163
Basic UDI-DI
8054083000V0AV103WN
EMDN code
Z12040292 General medicine therapeutic treatment instruments - medical device software
Device class
Class I
Special device type
Software
EU registration type
Standard device
EU market of registration
Austria

Manufacturer details

EUDAMED SRN
US-MF-000014055
Authorised representative
AbbVie Deutschland GmbH & Co. KG DE-AR-000007223

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Properties

Other properties (14, all answered No)