755 results
·
29ms
·
Sources: EU EUDAMED, US FDA
WARMAIR MODEL 135 HYPERTHERMIA SYSTEM (CONTROLLER AND BLANKETS)
FDA 510(k)
FDA Class 2
·Cardiovascular
LARGE CANNULATED SCREWS
FDA UDI
Smith & Nephew, Inc.·03596010064158·CANNULATED HIP PIN 105MM
PHYSICIAN'S DESKTOP REVIEW
FDA 510(k)
FDA Class 2
·Radiology
THERMODILUTION CATHETER
FDA 510(k)
FDA Class 2
·Cardiovascular
UNKNOWN
FDA Adverse Event
Injury
·WILLIAM COOK EUROPE·Product code DTK·August 14, 2015
MYNX CADENCE
FDA Adverse Event
Malfunction
·ACCESSCLOSURE, INC.·Product code MGB·April 19, 2013
CONSERVE(R) TOTAL A-CLASS(R) FEMORAL HEAD
FDA Adverse Event
Injury
·MICROPORT ORTHOPEDICS INC.·Product code JDL·September 26, 2014
ACS POLY 20D 28 GR3
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.·Product code LPH·June 2, 2011
UNKNOWN
FDA Adverse Event
Injury
·WILLIAM COOK EUROPE·Product code DTK·January 5, 2017
UNKNOWN
FDA Adverse Event
Malfunction
·WILLIAM COOK EUROPE·Product code DTK·December 15, 2015
UNKNOWN
FDA Adverse Event
Malfunction
·WILLIAM COOK EUROPE·Product code DTK·November 19, 2015
UNKNOWN
FDA Adverse Event
Injury
·WILLIAM COOK EUROPE·Product code DTK·June 17, 2016
UNKNOWN
FDA Adverse Event
Injury
·COOK INC·Product code DTK·June 13, 2016
UNKNOWN
FDA Adverse Event
Injury
·WILLIAM COOK EUROPE·Product code DTK·November 17, 2016
UNKNOWN
FDA Adverse Event
Injury
·WILLIAM COOK EUROPE·Product code DTK·September 27, 2016
UNKNOWN
FDA Adverse Event
Injury
·WILLIAM COOK EUROPE·Product code DTK·June 24, 2016
UNKNOWN
FDA Adverse Event
Death
·WILLIAM COOK EUROPE·Product code DTK·June 9, 2016
UNKNOWN
FDA Adverse Event
Injury
·WILLIAM COOK EUROPE·Product code DTK·March 1, 2016
UNKNOWN
FDA Adverse Event
Injury
·WILLIAM COOK EUROPE·Product code DTK·November 19, 2015
NC QUANTUM APEX
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code LOX·April 6, 2026