Home GUDID 00895160002793 Fluoro-Check TM COVID-19 Antigen Test
Primary DI 00895160002793
Brand Fluoro-Check TM COVID-19 Antigen Test
Company NANO-DITECH CORPORATION
Model TF-8150
Device description An in vitro diagnostic, a time resolved fluorescence lateral flow immunoassay for the qualitative detection of nucleocapsid antigen from SARS-CoV-2.
Published 2020-11-25
Public version status Update
Distribution status In Commercial Distribution
MRI safety Labeling does not contain MRI Safety Information
Single use true Product Codes# Code, Name table Code Name QMN Covid-19 Multi-Analyte Antigen Device
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class QMN Covid-19 Multi-Analyte Antigen Device Unknown N
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 00895160002793 Primary GS1 0 10895160002790 Unit of Use GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized, UPC-A table Source identifier GTIN-14 normalized UPC-A EAN-13 00895160002793 00895160002793 895160002793 0895160002793 10895160002790 10895160002790
GMDN Terms# Term, Definition table Term Definition SARS-CoV-2 antigen IVD, kit, rapid ICT, self-testing A collection of reagents and other associated materials intended to be used for the qualitative and/or (semi-)quantitative detection of antigens from severe acute respiratory syndrome-associated coronavirus 2 (SARS-CoV-2), the causative agent of coronavirus disease (COVID-19), in a clinical specimen within a short period, relative to standard laboratory testing procedures, using an immunochromatographic test (ICT) method [lateral flow test]. This is a rapid test intended to be used for self-testing by a layperson in the home or similar environment.
Regulatory Flags# DUNS number 126544316 Device count 20 Kit true Lot or batch true Manufacturing date on label true Expiration date on label true Other Devices From This Company# Other Devices Sharing Product Codes# Primary DI, Brand, Company table Primary DI Brand Company Product code Published 00850044118656 iHealth iHealth Labs Inc. QMN 2026-05-15 00816862026863 WELLlife™ WONDFO USA CO., LTD. QMN 2025-05-16 10816862026860 WELLlife™ WONDFO USA CO., LTD. QMN 2025-05-16 00816862026153 WELLlife™ WONDFO USA CO., LTD. QMN 2024-12-24 10816862026150 WELLlife™ WONDFO USA CO., LTD. QMN 2024-12-24 00816862024586 WELLlife™ WONDFO USA CO., LTD. QMN 2024-12-20 00816862024630 WELLlife™ WONDFO USA CO., LTD. QMN 2024-12-20 00816862024661 WELLlife™ WONDFO USA CO., LTD. QMN 2024-12-20 00816862024685 WELLlife™ WONDFO USA CO., LTD. QMN 2024-12-20 00816862024708 WELLlife™ WONDFO USA CO., LTD. QMN 2024-12-20 00816862024722 WELLlife™ WONDFO USA CO., LTD. QMN 2024-12-20 10816862024583 WELLlife™ WONDFO USA CO., LTD. QMN 2024-12-20 10816862024637 WELLlife™ WONDFO USA CO., LTD. QMN 2024-12-20 10816862024668 WELLlife™ WONDFO USA CO., LTD. QMN 2024-12-20 10816862024682 WELLlife™ WONDFO USA CO., LTD. QMN 2024-12-20 10816862024705 WELLlife™ WONDFO USA CO., LTD. QMN 2024-12-20 10816862024729 WELLlife™ WONDFO USA CO., LTD. QMN 2024-12-20 00816862024500 WELLlife™ WONDFO USA CO., LTD. QMN 2024-09-24 10816862024507 WELLlife™ WONDFO USA CO., LTD. QMN 2024-09-24 30810107290041 Flowflex Plus COVID-19 and Flu A/B Home Test ACON LABORATORIES, INC. QMN 2024-08-14 00850042559536 CorDx Tyfast CORETESTS, INC. QMN 2024-06-13 00850042559550 CorDx Tyfast CORETESTS, INC. QMN 2024-06-13 00850042559567 CorDx Tyfast CORETESTS, INC. QMN 2024-06-13 00850042559529 CorDx Tyfast CORETESTS, INC. QMN 2024-06-13 10850042559533 CorDx Tyfast CORETESTS, INC. QMN 2024-06-13 10850042559557 CorDx Tyfast CORETESTS, INC. QMN 2024-06-13 10850042559564 CorDx Tyfast CORETESTS, INC. QMN 2024-06-13 00850044118427 iHealth iHealth Labs Inc. QMN 2024-05-25 00850044118434 iHealth iHealth Labs Inc. QMN 2024-05-24 00850044118458 iHealth iHealth Labs Inc. QMN 2024-05-24