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BD Veritor™ Plus Analyzer 256066

by Becton, Dickinson and Company

Ref 256066

BD Veritor™ Plus Analyzer 256066 is a device classified as Class A in the EU and Class I in the US made by Becton, Dickinson and Company, registered in EUDAMED on 14 Jul 2026 (Basic UDI-DI 038290ELAGYZIN7F) and listed in FDA GUDID since 25 May 2018 (UDI-DI 00382902560661), active as of 26 Oct 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 26 Oct 2026.

Regulatory status

as of registry sync 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR EUDAMED Number038290ELAGYZIN7F Basic UDI-DI 00382902560661UDI-DIDate14 Jul 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00382902560661 UDI-DI Date25 May 2018ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 038290ELAGYZIN7F registered 14 Jul 2026 Active
  • FDA GUDID UDI-DI 00382902560661 listed 25 May 2018 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00382902560661
  2. Registered EUDAMED 038290ELAGYZIN7F

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  • Withdrawn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
Veritor EUDAMED
BD Veritor™ Plus Analyzer GUDID
Generic name
Photometric/spectroscopic immunoassay analyser IVD
Model / Ref / Catalog
256066
Primary DI / UDI-DI
00382902560661
Basic UDI-DI
038290ELAGYZIN7F
Direct marketing DI
00382902560661
FDA product code
JJQ
EMDN code
W0201069099 Various rapid test chemistry / immunochemistry instruments - other
GMDN term
Photometric/spectroscopic immunoassay analyser IVD
Device class
Class A EUDAMED
Class I GUDID
Regulation number
862.2300
EU registration type
Standard device
EU market of registration
Belgium
GUDID distribution status
In Commercial Distribution
Size
Length — 14.3 Centimeter
Height — 7.6 Centimeter
Width — 9 Centimeter

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device classEUDAMED
Class A
GUDID
Class I

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

Related devices

Category: Photometric/spectroscopic immunoassay analyser IVD

Similar devices in this category

Other devices filed under VARIOUS RAPID TEST CHEMISTRY / IMMUNOCHEMISTRY INSTRUMENTS - OTHER.

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Properties

  • Near-patient testing
  • Professional testing
  • IVD instrument
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Serial number
  • Expiration date
Other properties (18, all answered No)