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Alinity 07P5520

by Abbott

Ref 07P5520

Alinity 07P5520 is a glucose IVD (EU IVDD general IVD; FDA Class II; FDA product code CFR, Hexokinase, Glucose) made by Abbott, registered in EUDAMED on 30 Oct 2026 (Basic UDI-DI B-00380740135447) and listed in FDA GUDID since 11 Jul 2018 (UDI-DI 00380740135447), 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-00380740135447 Basic UDI-DI 00380740135447UDI-DIDate30 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00380740135447 UDI-DI Date11 Jul 2018ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-00380740135447 registered 30 Oct 2026 Active
  • FDA GUDID UDI-DI 00380740135447 listed 11 Jul 2018 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00380740135447
  2. Registered EUDAMED B-00380740135447

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  • Withdrawn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
Glucose IVD, kit, spectrophotometry
Device name
Glucose
Model / Ref / Catalog
07P5520
Primary DI / UDI-DI
00380740135447
Basic UDI-DI
B-00380740135447
FDA product code
CFR
EMDN code
W01010213 Glucose
GMDN term
Glucose IVD, kit, spectrophotometry
Device class
Class IVD General EUDAMED
Class II GUDID
Regulation number
862.1345
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: Glucose IVD, kit, spectrophotometry

Similar devices in this category

Other devices filed under GLUCOSE.

Other devices from Abbott

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Properties

  • Contains animal tissues or cells
  • Contains substances of microbial origin
  • Reagent
  • IVD kit
  • Professional testing
  • Prescription use
  • Convenience kit
  • Lot / batch number
  • Expiration date
Other properties (17, all answered No)