8 results
·
18ms
·
Sources: EU EUDAMED, US FDA
MICROSTAT 2
FDA 510(k)
FDA Class 1
·General Hospital
Polystar HK
FDA UDI
Merz Dental GmbH·D7091984485·anteriors; shade C2; mould 93 S
SUPPORT RING
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
KD ACTIVATED PARTIAL THROMBOPLASTIN TIME REAGENT
FDA 510(k)
FDA Class 2
·Hematology
FORTIFY DR, DF4 CONNECTOR
FDA Adverse Event
Malfunction
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·February 28, 2013
DEXTRUS 4136
FDA Adverse Event
Injury
·BIOTRONIK SE & CO. KG·Product code NVZ·February 1, 2011
REOCOR D
FDA Adverse Event
Malfunction
·BIOTRONIK SE & CO. KG·Product code OVJ·August 6, 2014
SCREW, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES USA·Product code HWC·April 14, 2015