26 results
·
25ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
MEDICON 2.4 MANDIBULAR RECONSTRUCTION PLATING SYSTEM
FDA 510(k)
FDA Class 2
·Dental
AIRCAST, MODEL #3011
FDA 510(k)
FDA Class 2
·Cardiovascular
MAMMOTOME HAND HELD PROBE, MODEL MHH8
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
OT ULTRA TEST STRIPS
FDA Adverse Event
Injury
·LIFESCAN, INC.·Product code NBW·October 6, 2010
OT ULTRA TEST STRIPS
FDA Adverse Event
Injury
·LIFESCAN, INC.·Product code NBW·September 27, 2010
COGNIS
FDA Adverse Event
Malfunction
·GUIDANT CRM CLONMEL IRELAND·Product code NIK·April 9, 2013
MAYFIELD MODIFIED SKULL CLAMP
FDA Adverse Event
Malfunction
·INTEGRA-OHIO, INC.·Product code HBL·February 25, 2011
INSIGNIA
FDA Adverse Event
Injury
·GUIDANT CRM CLONMEL IRELAND·Product code DXY·May 8, 2008
OT ULTRA TEST STRIPS
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·April 5, 2012
OT ULTRAMINI METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·January 18, 2012
OT ULTRA TEST STRIPS
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·October 6, 2011
OT ULTRA TEST STRIPS
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·February 10, 2012
OT ULTRA TEST STRIPS
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·February 10, 2012
OT ULTRA TEST STRIPS
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·November 29, 2010
OT ULTRA TEST STRIPS
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·April 25, 2011
25 G X 5/8 IN. BD ECLIPSE¿ NEEDLE
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code FMI·March 1, 2016
OT TEST STRIPS BLUE
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·July 27, 2011
OT ULTRA TEST STRIPS
FDA Adverse Event
Injury
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·November 23, 2012
OT ULTRA TEST STRIPS
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·April 21, 2011
OT ULTRAMINI ENHANCED METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·August 9, 2011