FDA UDI In Commercial Distribution 🇺🇸 United States

QuickVue™

DI: 30014613340751 · Model: 20518 · WONDFO USA CO., LTD.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
QuickVue™
Primary DI
30014613340751
Version / Model
20518
Catalog Number
20518
Company Name
WONDFO USA CO., LTD.
Labeler DUNS
849098897
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-10-31
Public Version
1
Public Version Date
2025-11-10
Public Version Status
New
Public Device Record Key
6a867e30-911c-4201-9082-f46e4b1eb9d7

Device Description

QuickVue™ Influenza+SARS Test

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
SCA Multi-Analyte Respiratory Virus Antigen Detection Test

GMDN Terms

Code Name
64770 Multiple-genus respiratory virus antigen IVD, kit, rapid ICT, clinical

Identifiers

Type ID
Primary 30014613340751
Package 50014613340755

Storage Conditions

Type
Handling Environment Temperature
Temperature Range
2 – 30 Degrees Celsius