291 results · 56ms · Sources: EU EUDAMED, US FDA

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Boston Scientific Cardiac Diagnostic Technologies, Inc.

FDA registration
Boston Scientific Cardiac Diagnostic Technologies, Inc.·4 products·🇺🇸 United States

Boston Scientific Cardiac Diagnostic Technologies, Inc.

FDA registration
Boston Scientific Cardiac Diagnostic Technologies, Inc.·4 products·🇺🇸 United States

COBAS® 4800 BRAF V600 MUTATION TEST

FDA Adverse Event
Malfunction ·ROCHE MOLECULAR SYSTEMS, INC. - BRANCHBURG·Product code OWD·May 24, 2024

2517506-2017-00415

FDA Adverse Event
Malfunction ·April 21, 2017

CT EXPRES

FDA Adverse Event
Injury ·BRACCO INJENEERING S.A.·Product code IZQ·April 21, 2026

SOUNDSTAR® ECO DIAGNOSTIC ULTRASOUND CATHETER

FDA Adverse Event
Death ·BIOSENSE WEBSTER INC·Product code OBJ·February 21, 2020

ID NOW COVID 19 ASSAY

FDA Adverse Event
Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·March 3, 2022

ID NOW COVID 19 ASSAY

FDA Adverse Event
Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC·Product code QJR·February 26, 2022

ID NOW COVID 19 ASSAY

FDA Adverse Event
Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·February 24, 2022

SOUNDSTAR ECO GE 8F CATHETER

FDA Adverse Event
Injury ·BIOSENSE WEBSTER INC.·Product code OBJ·September 26, 2019

ID NOW COVID-19 ASSAY

FDA Adverse Event
Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC·Product code QJR·May 17, 2021

ID NOW COVID-19 ASSAY

FDA Adverse Event
Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC·Product code QJR·May 17, 2021

ID NOW COVID-19 ASSAY

FDA Adverse Event
Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC·Product code QJR·May 17, 2021

ID NOW COVID-19

FDA Adverse Event
Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC·Product code QJR·December 3, 2021

ID NOW COVID-19 ASSAY

FDA Adverse Event
Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC·Product code QJR·May 17, 2021

ID NOW COVID-19

FDA Adverse Event
Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC·Product code QJR·December 3, 2021

ID NOW COVID 19 ASSAY

FDA Adverse Event
Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC·Product code QJR·February 26, 2022

ID NOW COVID 19 ASSAY

FDA Adverse Event
Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·March 3, 2022

ID NOW COVID 19 ASSAY

FDA Adverse Event
Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·March 3, 2022

ID NOW COVID 19 ASSAY

FDA Adverse Event
Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC·Product code QJR·February 26, 2022