10 results
·
20ms
·
Sources: EU EUDAMED, US FDA
MUELLER HINTON BROTH
FDA 510(k)
FDA Class 2
·Microbiology
Tiger Shark System
FDA UDI
Choice Spine, LP·00840996180481·28Lx11Wx13H TRIAL,TIGER SHARK STRAIGHT
EXPEDIUM SPINE SYSTEM, VIPER SYSTEM, VIPER 2 SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
APEX FIXATION PINS
FDA 510(k)
FDA Class 2
·Orthopedic
7900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS GMBH·Product code JAA·March 24, 2014
CONCERTO CRT-D DR
FDA Adverse Event
Injury
·MEDTRONIC MED REL, INC.·Product code NIK·October 31, 2012
ROTICULATOR ENDO DISSECT 5MM INSTRUMENT
FDA Adverse Event
Malfunction
·USSC PUERTO RICO·Product code GCJ·August 13, 2010
5.5 EXP VERSE UNITIZED SET SCR
FDA Adverse Event
Injury
·MEDOS INTERNATIONAL SÃ RL CH·Product code NKB·December 19, 2019
5.5 EXP VERSE SCR 6.0X45
FDA Adverse Event
Injury
·MEDOS INTERNATIONAL SÃ RL CH·Product code NKB·December 19, 2019
Unify, Sterile EO, Model #/ Part #: CD3231-40/100029240, 100030104, 100041904; CD3231-40Q/100029281, 100030124, 100041905; CD3235-40/100029256, 100029293, 100029307, 100031111, 100037047, 100048897, 100070009; CD3235-40Q/100029257, 100029294, 100029308, 100031059, 100037048, 100070010; CD3281-40Q/100056770; CD3297-40/100056933
FDA Enforcement
Class II
·Terminated·St Jude Medical Inc.·July 4, 2018