9 results
·
18ms
·
Sources: EU EUDAMED, US FDA
SUCTION CATHETER TRAYS
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
HUMANSCAN
FDA UDI
HUMANSCAN CO., LTD·08809476810142·L6-24-D Ultrasound Probe
HUMANSCAN
FDA UDI
HUMANSCAN CO.,LTD·08809476810296·L6-24-D Ultrasound Probe
INSULIN PEN NEEDLE
FDA 510(k)
FDA Class 2
·General Hospital
HERPES GROUP IGG
FDA 510(k)
FDA Class 2
·Microbiology
DEXTRUS 4136
FDA Adverse Event
Injury
·BIOTRONIK SE & CO KG·Product code NVZ·November 5, 2012
9900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·March 17, 2014
CORONARY CONTROL SYRINGE
FDA Adverse Event
Malfunction
·MERIT MEDICAL SYSTEMS, INC.·Product code FMF·September 10, 2010
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