9 results
·
26ms
·
Sources: EU EUDAMED, US FDA
SIMS DELTEC, INC. CATHETER REPLACEMENT CONNECTOR
FDA 510(k)
FDA Class 2
·General Hospital
IS4000 da Vinci EndoWrist Instruments
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
TSK SELECT Needle
FDA 510(k)
FDA Class 2
·General Hospital
ENDOWRIST
FDA Adverse Event
Malfunction
·INTUITIVE SURGICAL, INC·Product code NAY·April 22, 2020
PENTA
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·June 19, 2014
COMPRESSOR MINI
FDA Adverse Event
Malfunction
·MAQUET CRITICAL CARE AB·Product code BTI·February 6, 2013
COGNIS
FDA Adverse Event
Injury
·GUIDANT CRM CLONMEL IRELAND·Product code NIK·January 6, 2011
LARGE EX-FIX 11MM CRBN FBR ROD 250MM / MR-CONDITIONAL
FDA Adverse Event
Injury
·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code KTT·April 12, 2018
LARGE EX-FIX 11MM CRBN FBR ROD 300MM / MR-CONDITIONAL
FDA Adverse Event
Injury
·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code KTT·April 12, 2018