12 results
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28ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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RITE-ANGLE DISPOSABLE PROPHY ANGLES
FDA 510(k)
FDA Class 1
·Dental
DATASCOPE PERCOR STAT DL9.5 FR34CC INTRA-AORT BALL
FDA 510(k)
FDA Class 2
·Cardiovascular
VIDEO OTOSCOPE
FDA 510(k)
FDA Class 1
·Ear, Nose, Throat
PREMICATH PICC
FDA Adverse Event
Malfunction
·VYGON GMBH·Product code LJS·May 20, 2015
PREMICATH PICC
FDA Adverse Event
Malfunction
·VYGON GMBH·Product code LJS·May 22, 2015
PREMICATH
FDA Adverse Event
Malfunction
·VYGON GMBH·Product code LJS·April 20, 2015
PREMICATH
FDA Adverse Event
VYGON GMBH·Product code LJS·April 20, 2015
PREMICATH PICC
FDA Adverse Event
Malfunction
·VYGON GMBH·Product code LJS·June 3, 2015
PICK 3722066 1MM PT 90 DEG
FDA Adverse Event
Malfunction
·MEDTRONIC, INC.·Product code JYT·February 11, 2013
FORTIFY VR, DF-4 CONNECTOR
FDA Adverse Event
Injury
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·January 10, 2011
FLEXI-SEAL SIGNAL FECAL MANAGEMENT SYSTEM KIT
FDA Adverse Event
Injury
·CONVATEC INC.·Product code KNT·July 18, 2014
ev3 Pipeline Flex Embolization Device with Shield Technology. Sold OUS. For neurological endovascular use.
FDA Enforcement
Class I
·Terminated·Micro Therapeutics Inc, Dba Ev3 Neurovascular·April 1, 2020