20 results · 40ms · Sources: EU EUDAMED, US FDA

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3.0MM TI CANNULATED SCREW LONG THREAD/32MM

FDA Adverse Event
Malfunction ·SYNTHES USA·Product code HWC·June 12, 2014

3.0MM TI CANNULATED SCREW SHORT THREAD/32MM

FDA Adverse Event
Malfunction ·SYNTHE USA·Product code HWC·June 12, 2014

1.1MM THREADED GUIDE WIRE 150MM

FDA Adverse Event
Malfunction ·SYNTHES USA·Product code FZX·June 12, 2014

1.1MM THREADED GUIDE WIRE 150MM

FDA Adverse Event
Malfunction ·SYNTHES USA·Product code FZX·June 12, 2014

1.1MM THREADED GUIDE WIRE 150MM

FDA Adverse Event
Malfunction ·SYNTHES USA·Product code FZX·June 12, 2014

1.1MM THREADED GUIDE WIRE 150MM

FDA Adverse Event
Malfunction ·SYNTHES USA·Product code FZX·June 12, 2014

3.0MM TI CANNULATED SCREW SHORT THREAD/20MM

FDA Adverse Event
Malfunction ·SYNTHES USA·Product code HWC·June 12, 2014

1.1MM THREADED GUIDE WIRE 150MM

FDA Adverse Event
Malfunction ·SYNTHES USA·Product code FZX·June 12, 2014

2.0MM CANNULATED DRILL BIT/QC 150MM

FDA Adverse Event
Malfunction ·SYNTHES USA·Product code HWE·June 12, 2014

CRUCIFORM SCREWDRIVER SHAFT

FDA Adverse Event
Malfunction ·SYNTHES USA·Product code HXX·June 12, 2014

1.1MM NON-THREADED GUIDE WIRE 150MM

FDA Adverse Event
Malfunction ·SYNTHES USA·Product code FZX·June 12, 2014

3.0MM TI CANNULATED SCREW

FDA Adverse Event
Malfunction ·SYNTHES USA·Product code HWC·June 12, 2014

1.1MM THREADED GUIDE WIRE 150MM

FDA Adverse Event
Malfunction ·SYNTHES USA·Product code FZX·June 12, 2014

3.0MM TI CANNULATED SCREW SHORT THREAD/34MM

FDA Adverse Event
Malfunction ·SYNTHES USA·Product code HWC·June 12, 2014

1.1MM NON-THREADED GUIDE WIRE 150MM

FDA Adverse Event
Malfunction ·SYNTHES USA·Product code FZX·June 12, 2014

3.0MM TI CANNULATED SCREW SHORT THREAD/15MM

FDA Adverse Event
Malfunction ·SYNTHES USA·Product code HWC·June 12, 2014

3.0MM TI CANNULATED SCREW SHORT THREAD/15MM

FDA Adverse Event
Malfunction ·SYNTHES USA·Product code HWC·June 12, 2014

LYNX SYSTEM

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·February 14, 2013

DEPUY ASR XL FEM IMP SIZE 47

FDA Adverse Event
Injury ·DEPUY INTERNATIONAL LTD. 8010379·Product code KWA·January 7, 2011

OT VERIO IQ METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 29, 2014