13 results
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18ms
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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
UNICEL® DXC 600I SYNCHRON® ACCESS® CLINICAL SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER INC.·Product code JJE·June 1, 2011
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
CENTRIMAG 2ND GENERATION PRIMARY CONSOLE
FDA Adverse Event
Malfunction
·THORATEC SWITZERLAND GMBH·Product code DWA·September 28, 2022