11 results
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17ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
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SIMILAR DEVICE S7001, PMA # P990071
FDA Adverse Event
Malfunction
·STOCKERT GMBH·Product code LPB·November 13, 2014
SIMILAR DEVICE S7001, PMA # P990071
FDA Adverse Event
Malfunction
·STOCKERT GMBH·Product code LPB·March 10, 2016
SIMILAR DEVICE S7001, PMA # P990071
FDA Adverse Event
Malfunction
·STOCKERT GMBH·Product code LPB·August 31, 2017
SIMILAR DEVICE S7001, PMA # P990071
FDA Adverse Event
Malfunction
·STOCKERT GMBH·Product code LPB·May 19, 2016
CAPSURE SP NOVUS
FDA Adverse Event
Malfunction
·MPRI·Product code DTB·August 7, 2014
SPRINT QUATTRO SECURE
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO, INC.·Product code LWS·February 15, 2011
NGEN PUMP
FDA Adverse Event
Malfunction
·BIOSENSE WEBSTER INC·Product code LPB·March 31, 2026
STOCKERT
FDA Adverse Event
Malfunction
·STOCKERT GMBH·Product code BXN·September 14, 2015
ACUVUE ABILITI OVERNIGHT THERAPEUTIC LENSES FOR MYOPIA MANAGEMENT
FDA Adverse Event
Malfunction
·MENICON CO. LTD.·Product code NUU·January 2, 2024
NGEN PUMP
FDA Adverse Event
Malfunction
·BIOSENSE WEBSTER INC·Product code LPB·December 10, 2025
NGEN PUMP
FDA Adverse Event
Malfunction
·BIOSENSE WEBSTER INC·Product code LPB·December 16, 2025