14 results
·
19ms
·
Sources: EU EUDAMED, US FDA
CARDIOPULMONARY RESUSCITATOR
FDA 510(k)
FDA Class 2
·Cardiovascular
UNKNOWN BUR
FDA Adverse Event
Malfunction
·MEDTRONIC XOMED INC.·Product code EQJ·November 4, 2020
UNKNOWN BUR
FDA Adverse Event
Malfunction
·MEDTRONIC XOMED INC.·Product code EQJ·November 4, 2020
UNKNOWN BUR
FDA Adverse Event
Malfunction
·MEDTRONIC XOMED INC.·Product code EQJ·November 4, 2020
UNKNOWN BUR
FDA Adverse Event
Malfunction
·MEDTRONIC XOMED INC.·Product code EQJ·November 4, 2020
FORE-SIGHT ELITE ABSOLUTE TISSUE OXIMETER
FDA 510(k)
FDA Class 2
·Cardiovascular
VALIDATE TDM CALIBRATION VERIFICATION TEST SET, MODEL 126
FDA 510(k)
FDA Class 2
·Clinical Toxicology
XPS® BUR - UNKNOWN
FDA Adverse Event
Malfunction
·MEDTRONIC XOMED INC.·Product code EQJ·March 9, 2017
DRILL 3055601 SKEETER OTO-TOOL
FDA Adverse Event
Malfunction
·MEDTRONIC XOMED INC·Product code ERL·January 11, 2013
XPS® BUR - UNKNOWN
FDA Adverse Event
Malfunction
·MEDTRONIC XOMED INC.·Product code EQJ·March 8, 2017
ENDOVIVE? JEJUNAL FEEDING TUBE
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - SPENCER·Product code KNT·May 27, 2014
DISPOSABLE HEMOSTASIS CLIP
FDA Adverse Event
Malfunction
·WILSON-COOK MEDICAL INC·Product code MND·November 5, 2012
ATTAIN STARFIX
FDA Adverse Event
Malfunction
·MPRI·Product code OJX·June 10, 2015
Unify Quadra, Sterile EO, Model #/ Part #: CD3249-40/100036404, 100038435, CD3249-40Q/100036407, 100038436, CD3251-40/100036405, 100038095, 100038226, 100038437, 100038451, 100072563, CD3251-40Q/100036408, 100038214, 100038230, 100038407, 100038442, 100072564, CD3255-40/100038224, CD3255-40Q/100036514
FDA Enforcement
Class II
·Terminated·St Jude Medical Inc.·July 4, 2018