1,114 results
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24ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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UreTron PF Series Probe
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
REACH REVISION HIP SYSTEM
FDA UDI
Biomet Orthopedics, LLC·00880304251625·
REACH® REVISION HIP SYSTEM
FDA UDI
Biomet Orthopedics, LLC·00880304839236·
Heat Stress Component
FDA UDI
Certified Safety Manufacturing, Inc.·00766588121192·Heat Stress Component
REACH® REVISION HIP SYSTEM
FDA UDI
Biomet Orthopedics, LLC·00880304839144·
REACH® REVISION HIP SYSTEM
FDA UDI
Biomet Orthopedics, LLC·00880304839083·
MSI Precision Specialty Instruments
FDA UDI
Med Saver, Inc.·00194613122966·Inner Vent Instrument Guard, Clear, Non-Sterile...
REACH REVISION HIP SYSTEM
FDA UDI
Biomet Orthopedics, LLC·00880304222632·
REACH REVISION HIP SYSTEM
FDA UDI
Biomet Orthopedics, LLC·00880304007871·
REACH(R) FEMORAL PROVISIONAL
FDA UDI
Biomet Orthopedics, LLC·00880304306974·
SUR-G GLOV AND MAXITEX
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
HLR MODEL 601 HEART LUNG RESUSCITATOR AND HEARTSAVER 100
FDA 510(k)
FDA Class 2
·Cardiovascular
GUNTHER TULIP JUGULAR VENA CAVA FILTER SET
FDA Adverse Event
Injury
·COOK INC·Product code DTK·January 5, 2017
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDICS·Product code KWP·October 10, 2014
9600
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS·Product code JAA·June 3, 2013
VALIANT THORACIC STENT GRAFT WITH XCELERANT
FDA Adverse Event
Death
·MEDTRONIC CARDIOVASCULAR IRELAND·Product code MIH·July 8, 2011
UNKNOWN
FDA Adverse Event
Injury
·WILLIAM COOK EUROPE·Product code DTK·May 20, 2016
UNKNOWN
FDA Adverse Event
Injury
·WILLIAM COOK EUROPE·Product code DTK·August 14, 2015
UNKNOWN
FDA Adverse Event
Malfunction
·WILLIAM COOK EUROPE·Product code DTK·March 10, 2016
GUNTHER TULIP JUGULAR & FEMORAL VENA CAVA FILTER SET
FDA Adverse Event
Injury
·COOK INC·Product code DTK·February 9, 2017