10 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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HYDRAGEL BENCE JONES KIT/MAXI KIT HYDRAGEL BENCE JONES/HYDRAGEL 2/4 BENCE JONES KIT
FDA 510(k)
FDA Class 2
·Immunology
Fixed Patient Leads ECG Cable (Model 3153)
FDA 510(k)
FDA Class 2
·Cardiovascular
CARDIOP-B SYSTEM, VERSION 2.1
FDA 510(k)
FDA Class 2
·Radiology
IBP ELBOW INTERLOK FINISH ULNAR COMPONENT STANDARD LEFT
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code JDB·June 14, 2017
UNKNOWN KUDO ELBOW
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code JDB·February 9, 2017
UNKNOWN KUDO ELBOW
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code JDB·March 2, 2017
UNKNOWN KUDO ELBOW
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code JDB·February 9, 2017
GLIDESCOPE COBALT AVL MONITOR
FDA Adverse Event
Malfunction
·VERATHON MEDICAL (CANADA) ULC·Product code CCW·February 15, 2013
ONE TOUCH PING GLUCOSE MANAGEMENT SYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORP.·Product code LZG·January 13, 2011
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·August 1, 2014