97 results
·
53ms
·
Sources: EU EUDAMED, US FDA
Access Bio, Inc.
FDA registration
Access Bio, Inc.·10 products·🇺🇸 United States
CareSuperb COVID-19 Antigen Home Test
FDA UDI
Access Bio Inc.·00850010224435·
CareSuperb COVID-19/FluA&B Antigen Combo HomeTest
FDA UDI
Access Bio Inc.·00850010224374·
CareSuperb COVID-19/FluA&B Antigen Combo HomeTest
FDA UDI
Access Bio Inc.·00850010224350·
CareSuperb COVID-19 Antigen Home Test
FDA UDI
Access Bio Inc.·00850010224275·
CareSuperb COVID-19 Antigen Home Test
FDA UDI
Access Bio Inc.·00850010224305·
CareSuperb COVID-19/FluA&B Antigen Combo Home Test
FDA UDI
Access Bio Inc.·00850010224381·
CareSuperb COVID-19/FluA&B Antigen Combo HomeTest
FDA UDI
Access Bio Inc.·00850010224367·
ON/GO COVID-19 ANTIGEN SELF-TEST
FDA Adverse Event
Malfunction
·INTRIVO·Product code QKP·January 13, 2022
COVID-19 ANTIGEN SELF-TEST
FDA Adverse Event
Malfunction
·ACCESSS BIO, INCORPORATE·Product code QKP·January 19, 2022
CARESTART COVID-19 ANTIGEN (RHCM-02071)
FDA Adverse Event
Malfunction
·ACCESS BIO INCORPORATE·Product code QKP·February 8, 2022
ACCESSBIO CARESTART COVID-19 ANTIGEN HOME TEST
FDA Adverse Event
Malfunction
·ACCESS BIO, INC.·Product code QKP·September 23, 2025
CARESTART COVID 19 HOME TEST
FDA Adverse Event
Malfunction
·ACCESS BIO, INC.·Product code QKP·December 21, 2023
CARESTART COVID 19 HOME TEST
FDA Adverse Event
Malfunction
·ACCESS BIO, INC.·Product code QKP·December 21, 2023
ON/GO AT-HOME COVID-19 RAPID ANTIGEN SELF-TEST
FDA Adverse Event
Malfunction
·ACCESS BIO. INC·Product code QKP·February 17, 2022
UNICEL® DXC 600I SYNCHRON ® CHEMISTRY ANALYZER
FDA Adverse Event
Malfunction
·BECKMAN COULTER INC.·Product code JJE·January 10, 2011
UNICEL® DXC 660I SYNCHRON® ACCESS® CLINICAL SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER INC.·Product code JJE·September 17, 2010
*
FDA Adverse Event
Other
·BIOFORM MEDICAL, INC.·Product code LMH·March 4, 2005
ACCESS IMMUNOASSAY SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER INC.·Product code JJE·March 28, 2011
BINAXNOW COVID-19 AG SELF TEST 2CT
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QKP·September 23, 2024