68 results
·
23ms
·
Sources: EU EUDAMED, US FDA
MODIFIED OMNIWAVE ENDOVASCULAR SYSTEM
FDA 510(k)
FDA Class 2
·Cardiovascular
RESUSCITAIRE RADIANT WARMER; RESUSCITAIRE BIRTHING ROOM WARMER; RESUSCITAIR WALL MOUNTED RADIANT WARMER
FDA 510(k)
FDA Class 2
·General Hospital
QCS HER2 IMMUNOCONTROLS (PRODUCT NO. C010)
FDA 510(k)
FDA Class 2
·Hematology
ECHOTIP ULTRA ENDOSCOPIC ULTRASOUND NEEDLE
FDA Adverse Event
Injury
·COOK IRELAND LTD·Product code FCG·July 16, 2014
ECHOTIP ULTRA ENDOSCOPIC ULTRASOUND NEEDLE
FDA Adverse Event
Malfunction
·COOK IRELAND LTD·Product code FCG·October 25, 2018
ECHOTIP ULTRA ENDOSCOPIC ULTRASOUND NEEDLE
FDA Adverse Event
Malfunction
·COOK IRELAND LTD·Product code FCG·November 21, 2018
ECHOTIP ULTRA ENDOSCOPIC ULTRASOUND NEEDLE
FDA Adverse Event
Injury
·COOK IRELAND LTD·Product code FCG·November 27, 2018
FCG KIT, NEEDLE, BIOPSY
FDA Adverse Event
Injury
·COOK IRELAND LTD·Product code FCG·April 6, 2020
ECHOTIP ULTRA ENDOSCOPIC ULTRASOUND NEEDLE
FDA Adverse Event
Malfunction
·COOK IRELAND LTD·Product code FCG·January 8, 2019
ECHOTIP ULTRA ENDOSCOPIC ULTRASOUND NEEDLE
FDA Adverse Event
Malfunction
·COOK IRELAND LTD·Product code FCG·August 28, 2018
FCG KIT, NEEDLE, BIOPSY
FDA Adverse Event
Injury
·COOK IRELAND LTD·Product code FCG·April 6, 2020
FCG KIT, NEEDLE, BIOPSY
FDA Adverse Event
Injury
·COOK IRELAND LTD·Product code FCG·April 6, 2020
ECHOTIP ULTRA ENDOSCOPIC ULTRASOUND NEEDLE
FDA Adverse Event
Malfunction
·COOK IRELAND LTD·Product code FCG·June 28, 2019
ECHOTIP ULTRA ENDOSCOPIC ULTRASOUND NEEDLE
FDA Adverse Event
Injury
·COOK IRELAND LTD·Product code FCG·April 4, 2019
ECHOTIP ULTRA ENDOSCOPIC ULTRASOUND NEEDLE
FDA Adverse Event
Malfunction
·COOK IRELAND LTD·Product code FCG·September 6, 2018
ECHOTIP ULTRA ENDOSCOPIC ULTRASOUND NEEDLE
FDA Adverse Event
Malfunction
·COOK IRELAND LTD·Product code FCG·August 1, 2019
ECHOTIP ULTRA ENDOSCOPIC ULTRASOUND NEEDLE
FDA Adverse Event
Injury
·COOK IRELAND LTD·Product code FCG·July 12, 2019
ASR ACETABULAR IMPLANT 52
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL·Product code KWA·April 29, 2013
LTV
FDA Adverse Event
Malfunction
·CAREFUSION 203, INC.·Product code CBK·April 14, 2011
ACCU-CHEK AVIVA TEST STRIPS
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LFR·July 25, 2008