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Alinity 07P5730

by Abbott

Ref 07P5730

Alinity 07P5730 is an in vitro diagnostic device (EU IVDD general IVD; FDA Class II; FDA product code CJY, Azo Dye, Calcium) made by Abbott, registered in EUDAMED on 29 Oct 2026 (Basic UDI-DI B-00380740135409) and listed in FDA GUDID since 31 Aug 2018 (UDI-DI 00380740135409), active as of 7 Nov 2026.

Active European Union. Also listed in GUDID (US).

CE IVDD

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, GUDID, synced 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDD EUDAMED NumberB-00380740135409 Basic UDI-DI 00380740135409UDI-DIDate29 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00380740135409 UDI-DI Date31 Aug 2018ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-00380740135409 registered 29 Oct 2026 Active
  • FDA GUDID UDI-DI 00380740135409 listed 31 Aug 2018 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00380740135409
  2. Registered EUDAMED B-00380740135409

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/IVDD Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade name
Alinity
Generic name
Calcium (Ca2+) IVD, kit, spectrophotometry
Device name
Calcium
Model / Ref / Catalog
07P5730
Primary DI / UDI-DI
00380740135409
Basic UDI-DI
B-00380740135409
FDA product code
CJY
EMDN code
W01010303 Calcium
GMDN term
Calcium (Ca2+) IVD, kit, spectrophotometry
Device class
Class IVD General EUDAMED
Class II GUDID
Regulation number
862.1145
EU registration type
Legacy device (under a directive)
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device classEUDAMED
Class IVD General
GUDID
Class II

Device class is stated on each registry's own scale: Class IVD General in the EU (EUDAMED), Class II in the US (FDA GUDID). EU and US classes are different schemes, so this is not a disagreement.

Related devices

Category: Calcium (Ca2+) IVD, kit, spectrophotometry

Similar devices in this category

Other devices filed under CALCIUM.

Other devices from Abbott

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Properties

  • Reagent
  • IVD kit
  • Professional testing
  • Prescription use
  • Convenience kit
  • Lot / batch number
  • Expiration date
Other properties (19, all answered No)