30 results
·
28ms
·
Sources: EU EUDAMED, US FDA
OXYGEN THERAPY REGULATOR
FDA 510(k)
FDA Class 1
·Anesthesiology
Arthrex
FDA UDI
Provision·00810041061508·
Arthrex®
FDA UDI
ARTHREX, INC.·00888867052123·DRILL BIT, CANNULATED, 2.6MM
NA
FDA UDI
STERILMED, INC.·10888551012751·DRILL BIT CANNULATED
Arthrex
FDA UDI
Provision·B504OMAR8943020·
Reprocessed 2.6mm Cannulated Drill Bit
FDA UDI
SURETEK MEDICAL·B390AR8943021·
STAYFREE* DEODORANT MAXI-PADS
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
WAKO(TM) GOT II - HA
FDA 510(k)
FDA Class 2
·Clinical Chemistry
Arthrex®
FDA UDI
ARTHREX, INC.·00888867265738·2.6MM DRILL BIT, CANNULATED, REUSABLE
TAXUS EXPRESS2 PACLITAXEL-ELUTING CORONARY STENT SYSTEM
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC·Product code NIQ·June 21, 2007
7700
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS GMBH·Product code JAA·April 23, 2014
LINOX SD 65/18
FDA Adverse Event
Malfunction
·BIOTRONIK, INC.·Product code LWS·November 4, 2010
LIGASURE ATLAS HANDSWITCHING 37CM
FDA Adverse Event
Malfunction
·COVIDIEN LLC (SHANGHAI)·Product code GEI·November 16, 2012
RATCHETING ADAPTER, CANNULATED
FDA Adverse Event
Malfunction
·DEPUY SPINE INC·Product code LXH·April 12, 2021
RATCHETING ADAPTER, CANNULATED
FDA Adverse Event
Malfunction
·DEPUY SPINE INC·Product code LXH·July 25, 2023
LOW PROF SCRW,SS 4.0X 45MMCANN,SHT THD
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code HWC·September 27, 2023
DRV SFT,CANN,QC,T15 HEXALOBE
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code MDM·September 27, 2023
LO-PRO SCRW,TI,3.0MMX 20MMCORT
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code HWC·August 16, 2023
LO-PRO SCRW,TI,3.5MMX 12MM
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code HRS·August 17, 2023
3.0 X 14MM VAL SCREW, TI
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code HWC·August 17, 2023