7 results
·
19ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
CRANIOFACIAL ANCHORS
FDA 510(k)
FDA Class 2
·Orthopedic
De Soutter Medical
FDA UDI
DE SOUTTER MEDICAL LIMITED·05051471122987·K-WIRE - SINGLE TROCAR 1.25mm DIA x 150mm
PHOTIC STIMULATOR MODELS 580-PSCOMP,PSCEEG,PSSTAL
FDA 510(k)
FDA Class 2
·Neurology
SUTURE TENSION ADJUSTMENT REEL
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
VENACURE NEVERTOUCH
FDA Adverse Event
Injury
·ANGIODYNAMICS·Product code GEX·February 12, 2013
PARADIGM REAL-TIME INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·August 1, 2014
PRECISION TEST STRIPS
FDA Adverse Event
Malfunction
·ABBOTT DIABETES CARE, INC. USA·Product code NBW·January 31, 2011