15 results
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19ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
×
CAIMAN DISP.INSTR.NON ARTICUL. D: 5/360MM
FDA Adverse Event
Malfunction
·AESCULAP AG & CO. KG·Product code GEI·June 17, 2015
CAIMAN DISP. INSTR. NON ARTICUL. D:5/360 MM
FDA Adverse Event
Malfunction
·AESCULAP AG & CO. KG·Product code GEI·June 17, 2015
CAIMAN DISP.INSTR.NON ARTICUL. D:5/360MM
FDA Adverse Event
Malfunction
·AESCULAP AG & CO. KG·Product code GEI·June 17, 2015
CAIMAN DISP.INSTR.NON ARTICUL.D:5/360MM
FDA Adverse Event
Malfunction
·AESCULAP AG·Product code GEI·November 1, 2015
CAIMAN DISP. INSTR. NON ARTICUL.D:5 / 360MM
FDA Adverse Event
Malfunction
·AESCULAP AG & CO. KG·Product code GEI·August 13, 2015
CAIMAN DISP.INSTR.NON ARTICUL.D:5/360MM
FDA Adverse Event
Malfunction
·AESCULAP AG·Product code GEI·February 18, 2016
CAIMAN DISP. INSTR. NON ARTICUL. D:5/ 360MM
FDA Adverse Event
Malfunction
·AESCULAP AG AND CO. KG·Product code GEI·July 22, 2015
CAIMAN DISP.INSTR.NON ARTICUL.D:5/360MM
FDA Adverse Event
Malfunction
·AESCULAP AG & CO KG·Product code GEI·February 27, 2015
SYNCHRON® LX®I 725 CLINICAL SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER INC.·Product code JJE·June 1, 2011
VERSACARE
FDA Adverse Event
Malfunction
·HILL-ROM RITTER·Product code FNL·August 14, 2008
CAIMAN DISP.INSTR.NON ARTICUL.D:5/360MM
FDA Adverse Event
Malfunction
·AESCULAP AG·Product code GEI·April 20, 2016
CAIMAN DISP.INSTR.NON ARTICUL.D:5/360MM
FDA Adverse Event
Malfunction
·AESCULAP, INC.·Product code GEI·March 4, 2015
CAIMAN DISP.INSTR.NON ARTICUL.D:5/360MM
FDA Adverse Event
Malfunction
·AESCULAP AG·Product code GEI·February 17, 2016
TRI-STAPLE 2.0
FDA Adverse Event
Malfunction
·COVIDIEN LP LLC NORTH HAVEN·Product code GDW·February 13, 2024
LIBRE 2 SENSOR FREESTYLE
FDA Adverse Event
Malfunction
·ABBOTT DIABETES CARE INC·Product code QLG·February 9, 2024