2,952 results
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51ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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V4-I FB
FDA Adverse Event
Malfunction
·BHM MEDICAL, INC.·Product code FNG·November 13, 2009
IFB-DC-CO.CO-HS-00 (Interface Board)
FDA UDI
W & H Dentalwerk Bürmoos GmbH·J021303470001·Built-in Component
TALENT AAA
FDA Adverse Event
Injury
·MEDTRONIC CARDIOVASCULAR·Product code MIH·October 23, 2014
ENDURANT
FDA Adverse Event
Injury
·MEDTRONIC IRELAND·Product code MIH·October 23, 2014
ORGANOX METRA
FDA Adverse Event
Malfunction
·ORGANOX LIMITED·Product code QQK·May 28, 2026
RAIL SOCKET SIDE -- IF B/O SUGGEST ITEM #930749
FDA UDI
ALIMED, INC.·00733657239195·
EVIS LUCERA ULTRASONIC BRONCHOFIBERVIDEOSCOPE
FDA Adverse Event
Injury
·SHIRAKAWA OLYMPUS CO., LTD.·Product code PSV·April 18, 2023
SINGLE USE ASPIRATION NEEDLE NA-U401SX
FDA Adverse Event
Injury
·AOMORI OLYMPUS CO., LTD.·Product code FCG·April 18, 2023
EVIS EUS ULTRASOUND BRONCHOFIBERVIDEOSCOPE
FDA Adverse Event
Injury
·SHIRAKAWA OLYMPUS CO., LTD.·Product code PSV·April 18, 2023
BIOPSY FORCEPS
FDA Adverse Event
Injury
·AOMORI OLYMPUS CO., LTD.·Product code EOQ·April 18, 2023
FLUOROSCOPIC X-RAY
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·August 9, 2007
GE OEC 9600
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·February 17, 2009
FLUOROSCOPIC X-RAY
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·August 9, 2007
ORGANOX METRA
FDA Adverse Event
Malfunction
·ORGANOX LIMITED·Product code QQK·February 10, 2025
FLUOROSCOPIC X-RAY
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·November 30, 2007
9600
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·July 30, 2014
ORGANOX METRA
FDA Adverse Event
Malfunction
·ORGANOX LIMITED·Product code QQK·January 23, 2026
FLUOROSCOPIC X-RAY
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS INC·Product code JAA·August 22, 2007
ORGANOX METRA
FDA Adverse Event
Malfunction
·ORGANOX LIMITED·Product code QQK·December 23, 2025
GE OEC 9600
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS INC·Product code JAA·August 12, 2007