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QuickVue

FDA UDI

Class I (US FDA UDI)

by Quidel Corp.

Identity

Trade Name
QuickVue FDA UDI
Generic Name
Influenza A/B virus antigen IVD, kit, rapid ICT, clinical FDA UDI
Device Name
QkVue Flu A+B 20K-T, Bulk FDA UDI
Model / Reference
20189 FDA UDI
Description
QkVue Flu A+B 20K-T, Bulk FDA UDI

Identifiers

Catalog Number
20189 FDA UDI
Primary DI / UDI-DI
30014613331469 FDA UDI
FDA Product Code
GNX FDA UDI
GMDN Term
Influenza A/B virus antigen IVD, kit, rapid ICT, clinical FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
866.3330 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Influenza A/B virus antigen IVD, kit, rapid ICT, clinical

QuickVue by Quidel Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Influenza A/B virus antigen IVD, kit, rapid ICT, clinical.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Quidel Corp.

Sources (1)

  • FDA UDI 073040b7-6d1d-48d1-a3db-d50f734f2864 35 fields · synced Jun 6, 2026