8 results
·
26ms
·
Sources: EU EUDAMED, US FDA
BIO-LOGIC AUTOMATIC EVENT ANALYSIS
FDA 510(k)
FDA Class 2
·Neurology
De Soutter Medical
FDA UDI
DE SOUTTER MEDICAL LIMITED·05051471122758·K-WIRE - SINGLE TROCAR THREADED 1.5mm DIA x 100mm
MCCARTNEY ACCESS TUBE
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
Ellipse Supplemental Instrument Trays
FDA 510(k)
FDA Class 2
·General Hospital
TI COLLAR WITH GROOVES
FDA Adverse Event
Injury
·SYNTHES BRANDYWINE·Product code MNI·June 5, 2012
VIRTUOSO DR
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO OPERATIONS CO., JUNCOS·Product code LWS·February 9, 2013
ALTRUA
FDA Adverse Event
Injury
·GUIDANT CRM CLONMEL IRELAND·Product code NVZ·January 6, 2011
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 23, 2014