FDA.reportPublic FDA data

N/A

Primary DI
26977977230021
Brand
N/A
Company
Zhengzhou Shiyi Biotech Co., Ltd.
Model
A002
Device description
The COVID-19/Flu A&B Rapid Test is a rapid chromatographic immunoassay for the qualitative detection of COVID-19, Influenza A&B Antigen in Nasal swab. It is intended to aid in the rapid differential diagnosis of COVID-19,Influenza A and B
Published
2025-01-28
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
MR Safe
Rx
false
OTC
false
Sterile
true
Single use
true

Product Codes#

Code, Name table
CodeName
GNXAntigens, Cf (Including Cf Control), Influenza Virus A, B, C

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
GNXAntigens, Cf (Including Cf Control), Influenza Virus A, B, CMicrobiology1

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
26977977230021PackageGS1150In Commercial Distribution
16977977230024PrimaryGS10
06977977230027Unit of UseGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
2697797723002126977977230021
1697797723002416977977230024
06977977230027069779772300276977977230027

GMDN Terms#

Term, Definition table
TermDefinition
Multiple-genus respiratory virus antigen IVD, kit, rapid ICT, self-testingA collection of reagents and other associated materials intended to be used for the qualitative and/or (semi-)quantitative detection of antigens from multiple virus genera associated with respiratory disease in a clinical specimen within a short period, relative to standard laboratory testing procedures, using an immunochromatographic test (ICT) method [lateral flow test]. Viruses intended to be detected may include respiratory syncytial virus (RSV), influenza viruses, parainfluenza viruses, human metapneumovirus, coronaviruses, enteroviruses, rhinoviruses and/or adenoviruses. This is a rapid test intended to be used for self-testing by a layperson in the home or similar environment.

Sterilization Methods#

Method table
Method

Regulatory Flags#

DUNS number
456961760
Device count
2
DM exempt
false
Premarket exempt
true
HCT/P
false
Kit
false
Combination product
false
Lot or batch
true
Serial number
false
Manufacturing date on label
true
Expiration date on label
true
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
false
Sterilization required before use
false

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
16977977230024N/AA0022025-01-28
16977977230031N/AA0032025-01-28
26977977230038N/AA0032025-01-28

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
16977977230024N/AZhengzhou Shiyi Biotech Co., Ltd.GNX2025-01-28
16977977230031N/AZhengzhou Shiyi Biotech Co., Ltd.GNX2025-01-28
26977977230038N/AZhengzhou Shiyi Biotech Co., Ltd.GNX2025-01-28
05032384502981IMAGEN Influenza Virus A and BOXOID LIMITEDGNX2024-12-30
00855113008722ClearFitLONGEVITI NEURO SOLUTIONS LLCGNX2024-03-20
00855113008661Longeviti Convenience Kit 5.0LONGEVITI NEURO SOLUTIONS LLCGNX2024-03-15
08033891327514CHORUS INFLUENZA A IgGDIESSE DIAGNOSTICA SENESE SPAGNX2024-01-22
08033891327538CHORUS INFLUENZA B IgGDIESSE DIAGNOSTICA SENESE SPAGNX2024-01-22
00848838063701Remel REMEL, INC.GNX2021-11-12
30848838063702Remel REMEL, INC.GNX2021-11-12
03848838063708Remel REMEL, INC.GNX2021-11-12
00816917022925Poly statPOLYMEDCO, INC.GNX2019-04-18
30014613331469QuickVueQUIDEL CORPORATIONGNX2019-04-17
30014613003175QuickVueQUIDEL CORPORATIONGNX2019-03-21
30014613201830QuickVueQUIDEL CORPORATIONGNX2018-11-10
30014613202189SofiaQUIDEL CORPORATIONGNX2018-11-10
30014613202547SofiaQUIDEL CORPORATIONGNX2018-11-10
10743816001508Status Flu A+B cardPRINCETON BIOMEDITECH CORPORATIONGNX2018-07-05
00382902560708BD Veritor™ Plus Laboratory Combo PackBECTON, DICKINSON AND COMPANYGNX2018-05-25
00382902560739BD Veritor™ System Laboratory Combo PackBECTON, DICKINSON AND COMPANYGNX2018-05-25
00382902560746BD Veritor™ Plus CLIA-Waived Combo PackBECTON, DICKINSON AND COMPANYGNX2018-05-25
10743816001478BioSign Flu A+B cardPRINCETON BIOMEDITECH CORPORATIONGNX2018-04-09
10743816001447Status Flu A & BPRINCETON BIOMEDITECH CORPORATIONGNX2017-10-13
20612479225118McKessonMCKESSON MEDICAL-SURGICAL INC.GNX2017-09-29
20612479226795McKessonMCKESSON MEDICAL-SURGICAL INC.GNX2017-09-29
10743816001430Status Flu A+B Validation KitPRINCETON BIOMEDITECH CORPORATIONGNX2017-05-10
10743816001416Status Flu A+B Nasal Wash/Aspirate KitPRINCETON BIOMEDITECH CORPORATIONGNX2017-04-20
00382902560418BD Veritor™ System For Rapid Detection of Flu A+B Laboratory kitBECTON, DICKINSON AND COMPANYGNX2017-02-02
00382902560456BD Veritor™ System For Rapid Detection of Flu A+B CLIA-waived kitBECTON, DICKINSON AND COMPANYGNX2017-02-02
00742860100215OSOM Ultra Flu A&B Controls 5 TestSEKISUI DIAGNOSTICS, LLCGNX2017-01-10