FDA UDI In Commercial Distribution 🇺🇸 United States

CorDx Tyfast

DI: 00850042559550 · Model: ACT21002-2 · CORETESTS, INC.
Product Codes
1
GMDN Terms
2
Identifiers
3
Pkg Device Count
2

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
CorDx Tyfast
Primary DI
00850042559550
Version / Model
ACT21002-2
Company Name
CORETESTS, INC.
Labeler DUNS
036440919
Distribution Status
In Commercial Distribution
Device Count in Pkg
2
Record Status
Published
Publish Date
2024-06-13
Public Version
2
Public Version Date
2025-03-04
Public Version Status
Update
Public Device Record Key
d9f2e226-ce13-462d-b4b1-30bb0e85a833

Device Description

CorDx Tyfast Flu A/B & COVID-19 At Home Multiplex Rapid Test OTC

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
QMN Covid-19 Multi-Analyte Antigen Device

GMDN Terms

Code Name
49119 Influenza A/B virus antigen IVD, kit, rapid ICT, clinical
65454 SARS-CoV-2 antigen IVD, kit, rapid ICT, self-testing

Identifiers

Type ID
Package 10850042559557
Primary 00850042559550
Unit of Use 00850042559543