17 results
·
45ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Injury
×
MYO/WIRE II
FDA Adverse Event
Injury
·ALTO DEVELOPMENT CORP.·Product code GAQ·September 25, 2003
SUCTION COAGULATOR
FDA Adverse Event
Injury
·ALTO DEVELOPMENT CORP.·Product code GEI·July 18, 2014
ILLUMINATED DIRECT VIEW RETRACTOR
FDA Adverse Event
Injury
·ALTO DEVELOPMENT CORP·Product code GAD·December 13, 2005
MYO/WIRE II
FDA Adverse Event
Injury
·ALTO DEVELOPMENT CORP·Product code GAQ·December 27, 2001
MYO/WIRE
FDA Adverse Event
Injury
·ALTO DEVELOPMENT CORP.·Product code LDF·February 23, 2005
MYO/WIRE
FDA Adverse Event
Injury
·ALTO DEVELOPMENT CORP. A&E MEDICAL·Product code LDF·June 20, 1997
A&E MEDICAL 4.0 ROTATING SURGICAL PUNCH
FDA Adverse Event
Injury
·A&E MEDICAL / ALTO DEVELOPMENT CORP.·Product code LRY·December 22, 2020
MYO/WIRE
FDA Adverse Event
Injury
·A&E MEDICAL CORP./ALTO DEVELOPMENT CORP.·Product code IKD·March 25, 2026
NA
FDA Adverse Event
Injury
·ALTO DEVELOPMENT CORP., DBA A&E MEDICAL CORP.·Product code GEI·October 27, 2003
NA
FDA Adverse Event
Injury
·ALTO DEVELOPMENT CORP. / DBA A&E MEDICAL CORP.·Product code GEI·March 11, 2003
*
FDA Adverse Event
Injury
·ALTO DEVELOPMENT CORP./DBA A&E MEDICAL CORP.·Product code GEI·January 15, 2003
NA
FDA Adverse Event
Injury
·ALTO DEVELOPMENT CORP./DBA ACE MEDICAL CORP.·Product code GEI·March 7, 2003
MYO/WIRE
FDA Adverse Event
Injury
·ALTO DEVELOPMENT CORP. DBA A&E MEDICAL CORP.·Product code LDF·January 8, 2003
*
FDA Adverse Event
Injury
·ALTO DEVELOPMENT CORP./DBA A&E MEDICAL CORP.·Product code LDF·February 20, 2003
NA
FDA Adverse Event
Injury
·ALTO DEVELOPMENT CORP. DBA A&E MEDICAL CORP.·Product code GEI·April 23, 2004
SUCTION COAGULATOR
FDA Adverse Event
Injury
·ALTO DEVELOPMENT CORP., D/B/A A&E MEDICAL CORP.·Product code GEI·April 20, 2007
ACRYSOF RESTOR
FDA Adverse Event
Injury
·ALCON RESEARCH, LTD. / HUNTINGTON·Product code HQL·October 26, 2012