31 results
·
21ms
·
Sources: EU EUDAMED, US FDA
SIGMA DIAGNOSTICS AUTO D-DIMER CALIBRATOR, MODEL A7971
FDA 510(k)
FDA Class 2
·Hematology
NA
FDA UDI
Smith & Nephew, Inc.·03596010091062·13 MM CANNULATED DRILL BIT
SOLIDEA
FDA UDI
CALZIFICIO PINELLI SRL·08300496013549·MARILYN 30 SHEER, SIZE S, VISONE, GRADUATED COM...
ID NOW COVID-19 ASSAY
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·July 23, 2021
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033584712·
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033584729·
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033584767·
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033584705·
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033584743·
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033584736·
ID NOW COVID 19 ASSAY
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·May 14, 2021
ID NOW COVID-19 ASSAY
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·April 28, 2021
ID NOW COVID-19 ASSAY
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·April 28, 2021
ID NOW COVID 19 ASSAY
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·May 14, 2021
ID NOW COVID-19 ASSAY
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·April 8, 2021
ID NOW COVID-19 ASSAY
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·February 19, 2021
BILIARY AND PANCREATIC ENDOPROSTHESES (STENTS)
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
CODMAN CRANIOSORB ABSORBABLE FIXATION SYSTEM PURPLE RIVETS
FDA 510(k)
FDA Class 2
·Dental
RADIESSE DERMAL FILLER
FDA Adverse Event
Other
·BIOFORM MEDICAL, INC.·Product code LMH·July 15, 2009
LINER AND SHELL WITH PLASTIC BARRIER 48 MM I.D. 60 MM O.D.
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JDI·May 3, 2023