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QuickVue 20399

by Quidel Corp.

QuickVue 20399 is a device classified as Not classified made by Quidel Corp., listed in FDA GUDID since 30 Apr 2021 (UDI-DI 30014613339687), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number30014613339687 UDI-DI Date30 Apr 2021ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
QuickVue
Generic name
SARS-CoV-2 antigen IVD, kit, rapid ICT, self-testing
Model / Ref / Catalog
20399
Primary DI / UDI-DI
30014613339687
FDA product code
QKP
GMDN term
SARS-CoV-2 antigen IVD, kit, rapid ICT, self-testing
Device class
N
GUDID distribution status
In Commercial Distribution

Related devices

Category: SARS-CoV-2 antigen IVD, kit, rapid ICT, self-testing

Other devices from Quidel Corp.

See all devices from Quidel Corp. →

Properties

  • Single use
  • Over-the-counter
  • Convenience kit
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)