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Alinity 06P1270

by Abbott Ireland Diagnostics

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

Ref 06P1270

Alinity 06P1270 is a device classified as Class A (EU), Not classified (US) made by Abbott Ireland Diagnostics, registered in EUDAMED on 17 Aug 2026 (Basic UDI-DI 038074SLI0001T3) and listed in FDA GUDID since 18 Jul 2024 (UDI-DI 00380740157173), 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 Number038074SLI0001T3 Basic UDI-DI 00380740157173UDI-DIDate17 Aug 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00380740157173 UDI-DI Date18 Jul 2024ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 038074SLI0001T3 registered 17 Aug 2026 Active
  • FDA GUDID UDI-DI 00380740157173 listed 18 Jul 2024 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00380740157173
  2. Registered EUDAMED 038074SLI0001T3

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  • Withdrawn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
Chemiluminescent immunoassay oxidizing reagent IVD
Device name
Alinity i System Solutions
Model / Ref / Catalog
06P1270
Primary DI / UDI-DI
00380740157173
Basic UDI-DI
038074SLI0001T3
FDA product code
MZA, JJE
EMDN code
W0201020185 Automated immunochemistry analysers - consumables
GMDN term
Chemiluminescent immunoassay oxidizing reagent IVD
Device class
Class A EUDAMED
N GUDID
Regulation number
862.2160
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 A
GUDID
N

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

Related devices

Category: Chemiluminescent immunoassay oxidizing reagent IVD

Similar devices in this category

Other devices filed under AUTOMATED IMMUNOCHEMISTRY ANALYSERS - CONSUMABLES.

Other devices from Abbott Ireland Diagnostics

See all devices from Abbott Ireland Diagnostics →

Properties

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