15 results · 19ms · Sources: EU EUDAMED, US FDA

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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