FDA UDI In Commercial Distribution 🇺🇸 United States

COVID/Flu A&B RespiraDXTM Rapid Test

DI: B379RCFP251 · Model: RCFP-25 · INBIOS INTERNATIONAL, INC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
COVID/Flu A&B RespiraDXTM Rapid Test
Primary DI
B379RCFP251
Version / Model
RCFP-25
Catalog Number
RCFP-25
Company Name
INBIOS INTERNATIONAL, INC
Labeler DUNS
004006628
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-10-06
Public Version
2
Public Version Date
2026-03-26
Public Version Status
Update
Public Device Record Key
d565efb7-8278-42ac-b3e7-5bd7a7c95af5

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 B379RCFP251