11 results
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29ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ADVANCE PRESSURE MONITOR/HIGH PRESSURE LINES
FDA 510(k)
FDA Class 2
·Cardiovascular
OVER-THE-WIRE EXPANDABLE LEMAITRE VALVULOTOME
FDA 510(k)
FDA Class 2
·Cardiovascular
POWDERED SYNTHETIC VINYL PATIENT EXAMINATION GLOVES
FDA 510(k)
FDA Class 1
·General Hospital
COBALT CHROME FEMORAL HEAD SZ 28 3.5MM 12/14 SHORT NECK
FDA Adverse Event
Malfunction
·BIOMET UK LTD.·Product code JDI·December 15, 2016
COCR HEAD SHORT NECK DIA28/-3. 5 MM 12/14
FDA Adverse Event
Injury
·BIOMET FRANCE S.A.R.L.·Product code JDI·May 10, 2016
BIOMET COBALT-CHROME FEMORAL COMPONENTS
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code JDI·March 17, 2017
COBALT CHROME FEMORAL HEAD
FDA Adverse Event
Death
·BIOMET FRANCE S.A.R.L.·Product code JDI·August 31, 2017
9800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·May 13, 2014
ONE TOUCH PING GLUCOSE MANAGEMENT SYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·November 23, 2010
ENDOTAK ENDURANCE
FDA Adverse Event
Malfunction
·CPI - DEL CARIBE·Product code NVY·January 11, 2013
BIOMET COBALT-CHROME FEMORAL COMPONENTS
FDA Adverse Event
Injury
·BIOMET FRANCE S.A.R.L.·Product code JDI·April 7, 2017