6 results
·
17ms
·
Sources: EU EUDAMED, US FDA
STRATUS PROGESTERONE FLOUROMETRIC IMMUNOASSAY
FDA 510(k)
FDA Class 1
·Clinical Chemistry
MODIFICATION TO EBI XFIX VISION FIXATION SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
EASYPOINT NEEDLE
FDA 510(k)
FDA Class 2
·General Hospital
ASR UNI FEMORAL IMPL SIZE 49
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL, LTD·Product code KWA·December 17, 2010
ATLANTIS ANTERIOR CERVICAL PLATE SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWQ·January 29, 2013
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 15, 2014