FDA UDI In Commercial Distribution 🇺🇸 United States

Rapid Response

DI: 10722066009595 · Model: COF-19CGHU1 · BTNX Inc
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Rapid Response
Primary DI
10722066009595
Version / Model
COF-19CGHU1
Company Name
BTNX Inc
Labeler DUNS
251005005
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-05-29
Public Version
1
Public Version Date
2025-06-06
Public Version Status
New
Public Device Record Key
290069d5-0cf9-42c0-a84c-2793afb4d740

Device Description

Rapid Response Influenza AB + COVID-19 Antigen Detection Test (Anterior Nasal Swab)

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
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
66040 Multiple-genus respiratory virus antigen IVD, kit, rapid ICT, self-testing

Identifiers

Type ID
Primary 10722066009595