42 results
·
24ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
ETHANOL
FDA 510(k)
FDA Class 2
·Clinical Toxicology
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450522523·
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033514092·
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033514054·
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033514061·
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033514108·
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033514078·
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033514085·
Phonak
FDA UDI
Phonak AG·07613275085905·Phonak Naída Q90-SP (purple transparent)
ID NOW COVID-19 ASSAY
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·July 31, 2021
ID NOW COVID-19 ASSAY
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·May 13, 2021
ID NOW COVID-19 ASSAY
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·April 9, 2021
ID NOW COVID 19 ASSAY
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·August 23, 2021
ID NOW COVID-19
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·March 7, 2021
ID NOW COVID-19
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·February 24, 2021
ID NOW COVID-19 ASSAY
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·February 25, 2021
ID NOW COVID-19
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·March 7, 2021
ID NOW COVID-19
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·March 7, 2021
BINAX NOW COVID-19 AG CARD
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS SCARBOROUGH INC.·Product code QKP·February 11, 2021
ID NOW COVID-19 ASSAY
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·March 8, 2021