10 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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MEMOMETAL INTRA-MEDULLARY BONE FASTENER, MODELS SMART TOE / X-FUSE
FDA 510(k)
FDA Class 2
·Orthopedic
SYNOVIALSCOPICS, SYNOVIAL FLUID CONTROL
FDA 510(k)
FDA Class 2
·Hematology
5F GUIDING CATHETER
FDA 510(k)
FDA Class 2
·Cardiovascular
LUX 1440
FDA Adverse Event
Malfunction
·PALOMAR MEDICAL TECHNOLOGIES, INC.·Product code GEX·May 5, 2012
840 VENTILATOR
FDA Adverse Event
Malfunction
·COVIDIEN, FORMERLY NELLCOR·Product code CBK·April 17, 2013
PELORIS RAPID TISSUE PROCESSOR
FDA Adverse Event
Malfunction
·LEICA BIOSYSTEMS MELBOURNE·Product code IEO·April 14, 2011
GYNECARE MORCELLEX TISSUE MORCELLATOR
FDA Adverse Event
Malfunction
·ETHICON, INC.·Product code HET·July 2, 2008
BD INSULIN SYRINGE WITH THE BD ULTRA-FINE NEEDLE
FDA Adverse Event
Injury
·BD MEDICAL - DIABETES CARE·Product code FMF·November 6, 2019
SYRINGE 0.3ML 31GA 8MM TW 10BAG 500 CA
FDA Adverse Event
Injury
·BD MEDICAL - DIABETES CARE·Product code FMF·November 14, 2019
BD ULTRA-FINE INSULIN SYRINGE
FDA Adverse Event
Malfunction
·BD MEDICAL - DIABETES CARE·Product code FMF·October 25, 2019