10,000 results
·
70ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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CUSTOM DEFINED PRODUCT
FDA Adverse Event
Malfunction
·EDWARDS LIFESCIENCES DR·Product code DXO·October 21, 2014
OPUS
FDA Adverse Event
Malfunction
·DORNIER MEDIZINTECHNIK GMBHH·Product code KQS·January 18, 2002
FR2
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS, HEARTSTREAM·Product code MKJ·July 13, 2010
HEARTSTART ONSITE
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS (HTST)·Product code MKJ·December 28, 2011
HEARTSTART ONSITE
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS (HTST)·Product code MKJ·December 29, 2011
HEARTSTRING ONSITE
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS (HTST)·Product code MKJ·December 29, 2011
CHARITE ENDPLATE SIZE UNKNOWN
FDA Adverse Event
Malfunction
·DEPUY SPINE, INC.·Product code MJO·April 11, 2006
WAVELIGHT FS200 FEMTOSECOND LASER
FDA Adverse Event
Injury
·WAVELIGHT GMBH·Product code OOE·September 1, 2015
INTERA 3000
FDA Adverse Event
Malfunction
·INTERA ONCOLOGY·Product code LKK·December 16, 2022
MAGNA PURE LC INSTRUMENT
FDA Adverse Event
Malfunction
·PRECISION SYSTEMS SCIENCES·Product code JJE·November 12, 2004
V60 VENTILATOR
FDA Adverse Event
Malfunction
·RESPIRONICS CALIFORNIA, INC·Product code MNT·August 16, 2017
PERI-GUARD
FDA Adverse Event
Injury
·BIO-VASCULAR, INC.·Product code FTL·December 13, 1996
HANDPIECE MICS
FDA Adverse Event
Malfunction
·MAKO SURGICAL CORP.·Product code OLO·January 13, 2023
TRULIGN TORIC POSTERIOR CHAMBER IOL
FDA Adverse Event
Injury
·BAUSCH + LOMB·Product code MJP·June 12, 2015
CRYSTALENS ACCOMMODATING IOL
FDA Adverse Event
Injury
·BAUSCH + LOMB·Product code NAA·June 12, 2015
CRYSTALENS ACCOMMODATING IOL
FDA Adverse Event
Injury
·BAUSCH + LOMB·Product code NAA·December 20, 2016
CRYSTALENS HD IOL
FDA Adverse Event
Injury
·BAUSCH + LOMB·Product code NAA·May 23, 2012
CRYSTALENS
FDA Adverse Event
Injury
·BAUSCH + LOMB·Product code NAA·July 20, 2011
EVIS EXERA III DUODENOVIDEOSCOPE
FDA Adverse Event
Malfunction
·AIZU OLYMPUS CO., LTD.·Product code FDT·April 20, 2026
HEARTSINE SAMARITAN 200P AND PAD PAK
FDA Adverse Event
Malfunction
·HEARTSINE TECHNOLOGIES, LTD CANBERRA HOUSE·Product code MKJ·January 23, 2015