9 results
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22ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
HEMOCHRON CONTROL ACT TEST TUBE NORMAL/ABNOR. I/II
FDA 510(k)
FDA Class 2
·Hematology
Henry Schein
FDA UDI
HENRY SCHEIN, INC.·H65888824811·Amino Tray
HEM-6410T-ZM Wrist Blood Pressure Monitor
FDA 510(k)
FDA Class 2
·Cardiovascular
FLOWPICC CATHETER
FDA 510(k)
FDA Class 2
·General Hospital
TRANSTAR 84 IN SINGLE MONITORING KIT
FDA Adverse Event
Malfunction
·SMITHS MEDICAL ASD, INC.·Product code DPT·October 21, 2010
HI-TORQUE BALANCE MIDDLEWEIGHT ELITE GUIDE WIRE
FDA Adverse Event
Malfunction
·AV-TEMECULA-CT·Product code DQX·December 20, 2012
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·June 18, 2014
ESSURE
FDA Adverse Event
Injury
·BAYER PHARMA AG·Product code HHS·October 2, 2019
ESSURE
FDA Adverse Event
Injury
·BAYER PHARMA AG·Product code HHS·August 22, 2017