Skip to content

Alinity 07P5320

by Abbott

Ref 07P5320

Alinity 07P5320 is a buffered sample diluent IVD (EU IVDR Class C; FDA Class II) made by Abbott, registered in EUDAMED on 26 Oct 2026 (Basic UDI-DI 038074ACP0753HX) and listed in FDA GUDID since 30 May 2018 (UDI-DI 00380740121686), active as of 7 Nov 2026.

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

CE IVDR

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/IVDR EUDAMED Number038074ACP0753HX Basic UDI-DI 00380740121686UDI-DIDate26 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00380740121686 UDI-DI Date30 May 2018ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 038074ACP0753HX registered 26 Oct 2026 Active
  • FDA GUDID UDI-DI 00380740121686 listed 30 May 2018 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00380740121686
  2. Registered EUDAMED 038074ACP0753HX

Coverage

2 jurisdictions

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  • Withdrawn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

Specification

EUDAMED · GUDID

Trade name
Alinity
Generic name
Buffered sample diluent IVD
Model / Ref / Catalog
07P5320
Primary DI / UDI-DI
00380740121686
Basic UDI-DI
038074ACP0753HX
FDA product code
CEM, CGZ, JGS
EMDN code
W0101070302 Electrolyte electrode buffers and solutions
GMDN term
Buffered sample diluent IVD
Device class
Class C EUDAMED
Class II GUDID
Regulation number
862.1600, 862.1170, 862.1665
EU registration type
Standard device
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device classEUDAMED
Class C
GUDID
Class II

Device class is stated on each registry's own scale: Class C 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: Buffered sample diluent IVD

Similar devices in this category

Other devices filed under ELECTROLYTE ELECTRODE BUFFERS AND SOLUTIONS.

Other devices from Abbott

See all devices from Abbott →

Properties

  • Contains animal tissues or cells
  • Reagent
  • IVD kit
  • Professional testing
  • Prescription use
  • Convenience kit
  • Lot / batch number
  • Expiration date
Other properties (18, all answered No)