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Alinity

by Abbott Laboratories 11 variants

Part of a family of 9 devices: see the family page

Ref 08P9671

Alinity (08P9671) is a Class A device made by Abbott Laboratories, registered in EUDAMED on 29 Oct 2026 (Basic UDI-DI 038074DAL0006FY), active as of 7 Nov 2026.

Active European Union

CE IVDR

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 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number038074DAL0006FY Basic UDI-DI 00380740191641UDI-DIDate29 Oct 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  • Withdrawn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/IVDR Active

Specification

EUDAMED

Device name
Alinity c System Solutions
Model / reference
08P9671
Primary DI / UDI-DI
00380740191641
Basic UDI-DI
038074DAL0006FY
EMDN code
W0201010185 Chemistry analysers - consumables
Device class
Class A
EU registration type
Standard device
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
US-MF-000017777
Authorised representative
Abbott GmbH DE-AR-000009457

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Properties

  • Professional testing
  • IVD instrument
Other properties (11, all answered No)