19 results
·
54ms
·
Sources: EU EUDAMED, US FDA
PNEUPAC FIRST RESPONDER WITHOUT ALARMS
FDA Adverse Event
Malfunction
·SMITHS MEDICAL PM, INC.·Product code BTL·June 26, 2009
NEURX DIAPHRAGM PACING SYSTEM
FDA Adverse Event
Death
·SYNAPSE BIOMEDICAL INC.·Product code OIR·May 3, 2016
DIALOG A + HE/BIC
FDA Adverse Event
Injury
·B. BRAUN AVITUM AG - MELSUNGEN·Product code FKJ·July 22, 2016
PNEUPAC PARAPAC WITHOUT ALARMS
FDA Adverse Event
Malfunction
·SMITHS MEDICAL PM, INC.·Product code BTL·May 23, 2009
KION
FDA Adverse Event
Injury
·MAQUET CRITICAL CARE AB·Product code BSZ·February 1, 2007
PNEUPAC PARAPAC WITHOUT ALARMS
FDA Adverse Event
Death
·SMITHS MEDICAL PM, INC.·Product code BTL·April 3, 2009
BEAR III
FDA Adverse Event
BEAR MEDICAL SYSTEMS INC.·Product code BTL·May 17, 1993
DIALOG+®
FDA Adverse Event
Malfunction
·B. BRAUN AVITUM AG·Product code KDI·April 12, 2023
DIALOG+®
FDA Adverse Event
Malfunction
·B. BRAUN AVITUM AG·Product code KDI·April 12, 2023
DIALOG+®
FDA Adverse Event
Malfunction
·B. BRAUN AVITUM AG·Product code KDI·April 12, 2023
DIALOG+®
FDA Adverse Event
Malfunction
·B. BRAUN AVITUM AG·Product code KDI·April 12, 2023
DIALOG+®
FDA Adverse Event
Malfunction
·B. BRAUN AVITUM AG·Product code KDI·April 11, 2023
DIALOG+®
FDA Adverse Event
Malfunction
·B. BRAUN AVITUM AG·Product code KDI·April 11, 2023
DIALOG+®
FDA Adverse Event
Malfunction
·B. BRAUN AVITUM AG·Product code KDI·April 12, 2023
DIALOG+®
FDA Adverse Event
Malfunction
·B. BRAUN AVITUM AG·Product code KDI·April 12, 2023
DIALOG+®
FDA Adverse Event
Malfunction
·B. BRAUN AVITUM AG·Product code KDI·April 12, 2023
DIALOG+®
FDA Adverse Event
Malfunction
·B. BRAUN AVITUM AG·Product code KDI·April 11, 2023
DIALOG+®
FDA Adverse Event
Malfunction
·B. BRAUN AVITUM AG·Product code KDI·April 11, 2023
Wellkang Ltd
Authorized representative
259 Manufacturers·3500 Devices