24 results
·
20ms
·
Sources: EU EUDAMED, US FDA
WEISS RETINAL CANNULA
FDA 510(k)
FDA Class 1
·Ophthalmic
Endo Carry-on Procedure Kit
FDA UDI
MEDIVATORS INC.·00677964150074·Endo Carry-on Procedure Kit Includes Basin, Def...
Axcent Acrylics
FDA UDI
GARRECO, LLC·D79330103050·DNT BASE REPR DK FIBER SC 5 LBS
GLACIER
FDA UDI
SDI LIMITED·DO3670103051·
Oxygen Sensor
FDA UDI
MERCURY ENTERPRISES, INC.·10641043103050·
Ovation Tribute Hip Stem
FDA UDI
Ortho Development Corporation·00822409010981·STD SIZE 5 Stem Plasma Spray
9616240-2006-00344
FDA Adverse Event
Malfunction
·Product code KDI·June 14, 2006
9616240-2006-00342
FDA Adverse Event
Malfunction
·Product code KDI·June 14, 2006
9616240-2006-00330
FDA Adverse Event
Malfunction
·Product code FII·June 1, 2006
MAC-LAB SYSTEM AND CARDIOLAB EP SYSTEM
FDA 510(k)
FDA Class 2
·Cardiovascular
HARDYDISK, CEFOXITIN, 30MCG
FDA 510(k)
FDA Class 2
·Microbiology
9616240-2006-00349
FDA Adverse Event
Malfunction
·Product code FII·June 21, 2006
9616240-2006-00348
FDA Adverse Event
Malfunction
·Product code FDI·June 20, 2006
*
FDA Adverse Event
Malfunction
·Product code FII·June 1, 2006
BD VACUTAINER® LH 68 I.U. PLUS BLOOD COLLECTION TUBES
FDA Adverse Event
Malfunction
·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·May 30, 2023
9616240-2006-00346
FDA Adverse Event
Malfunction
·Product code FII·June 14, 2006
FREESTYLE FLASH
FDA Adverse Event
Malfunction
·ABBOTT DIABETES CARE INC, USA·Product code LFR·May 11, 2007
JUVEDERM (VOLUME/CONCENTRATION UNKNOWN)
FDA Adverse Event
Injury
·ALLERGAN·Product code LMH·March 14, 2013
PYXIS ANESTHESIA SYSTEM (PAS)
FDA Adverse Event
Malfunction
·CAREFUSION·Product code BRY·February 11, 2011
Kendall MONOJECT MAGELLAN SAFETY NEEDLE 21G X 1 inch Product Number: 5551850110
FDA Recall
Terminated
·Kendall Healthcare Products Co·Product code FMI·October 8, 2004