24 results
·
19ms
·
Sources: EU EUDAMED, US FDA
PERIKON PCL 90
FDA 510(k)
FDA Class 1
·Ophthalmic
5922294
FDA Adverse Event
Malfunction
·September 1, 2016
APNEACHECK
FDA 510(k)
FDA Class 2
·Anesthesiology
PRESSURIZED INFUSION PUMP
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
IMMAGE® RHEUMATOID FACTOR REAGENT
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code DHR·March 21, 2012
IMMAGE® RHEUMATOID FACTOR REAGENT
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code DHR·January 13, 2012
IMMAGE® RHEUMATOID FACTOR REAGENT
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code DHR·January 13, 2012
IMMAGE® RHEUMATOID FACTOR REAGENT
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code DHR·February 1, 2012
IMMAGE® RHEUMATOID FACTOR REAGENT
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code DHR·January 6, 2012
IMMAGE® RHEUMATOID FACTOR REAGENT
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code DHR·March 21, 2012
IMMAGE® RHEUMATOID FACTOR REAGENT
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code DHR·March 21, 2012
IMMAGE® RHEUMATOID FACTOR REAGENT
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code DHR·January 13, 2012
IMMAGE® RHEUMATOID FACTOR REAGENT
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code DHR·December 22, 2011
SPRINT QUATTRO SECURE
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO, INC.·Product code LWS·December 13, 2010
MONARC SLING SYSTEM
FDA Adverse Event
Injury
·AMERICAN MEDICAL SYSTEMS, INC.·Product code FTL·January 11, 2013
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·July 9, 2014
IMMAGE® RHEUMATOID FACTOR REAGENT
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code DHR·January 30, 2012
IMMAGE® RHEUMATOID FACTOR REAGENT
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code DHR·January 30, 2012
IMMAGE® RHEUMATOID FACTOR REAGENT
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code DHR·January 6, 2012
IMMAGE® RHEUMATOID FACTOR REAGENT
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code DHR·January 6, 2012