18 results · 28ms · Sources: EU EUDAMED, US FDA

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9616026-2006-00240

FDA Adverse Event
Malfunction ·Product code FII·June 21, 2006

9616026-2006-00244

FDA Adverse Event
Malfunction ·Product code FII·June 22, 2006

9616026-2006-00239

FDA Adverse Event
Malfunction ·Product code FII·June 22, 2006

9616026-2006-00222

FDA Adverse Event
Malfunction ·Product code FII·June 21, 2006

PRISMAFLEX SYSTEM

FDA Adverse Event
Malfunction ·GAMBRO LUNDIA AB, MONITOR DIVISION·Product code MQS·June 8, 2006

PRISMAFLEX SYSTEM

FDA Adverse Event
Malfunction ·GAMBRO LUNDIA AB, MONITOR DIVISION·Product code MQS·June 8, 2006

PRISMAFLEX SYSTEM

FDA Adverse Event
Malfunction ·GAMBRO LUNDIA AB, MONITOR DIVISION·Product code MQS·June 8, 2006

9616026-2006-00252

FDA Adverse Event
Other ·Product code FII·June 21, 2006

9616026-2006-00245

FDA Adverse Event
Malfunction ·Product code FII·June 22, 2006

9616026-2006-00253

FDA Adverse Event
Other ·Product code FII·June 21, 2006

PRISMAFLEX SYSTEM

FDA Adverse Event
Malfunction ·GAMBRO LUNDIA AB, MONITOR DIVISION·Product code MQS·June 8, 2006

9616026-2006-00221

FDA Adverse Event
Malfunction ·Product code FII·June 21, 2006

PRISMAFLEX SETS (M)

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code KDI·May 13, 2024

REZOOM

FDA Adverse Event
Injury ·ABBOTT MEDICAL OPTICS·Product code MFK·December 28, 2010

ANIMAS INSULIN INFUSION PUMP

FDA Adverse Event
Malfunction ·ANIMAS CORPORATION·Product code LZG·April 8, 2013

PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

FDA Adverse Event
Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·August 27, 2014

ENDOTAK RELIANCE

FDA Adverse Event
Injury ·CPI - DEL CARIBE·Product code NVY·April 6, 2011

PRISMAFLEX SETS (M & ST)

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code KDI·March 28, 2023