9 results
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18ms
·
Sources: EU EUDAMED, US FDA
CR-39 PLASTIC LENSES FOR EYEGLASSES
FDA 510(k)
FDA Class 1
·Ophthalmic
dentaform®
FDA UDI
DENTAURUM GmbH & Co.KG·J011882308220·dentaform® Band, tooth 16, size 8/Roth 22
dentaform®
FDA UDI
DENTAURUM GmbH & Co.KG·J011882308180·dentaform® Band, tooth 16, size 8/Roth 18
Non-Sterile, Powder-Free Nitrile Examination Glove Pink Tested for use with Chemotherapy Drugs
FDA 510(k)
FDA Class 1
·General Hospital
MODIFICATION TO VIGILEO ARTERIAL PRESSURE CARDIAC OUTPUT/OXIMETRY MONITOR
FDA 510(k)
FDA Class 2
·Cardiovascular
UNIV 2-HOLE SHL 56MM LNR SZ 24
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code MEH·June 18, 2014
SCULPTRA
FDA Adverse Event
Injury
·SANOFI AVENTIS U.S. LLC·Product code LMH·October 22, 2010
STEALTHSTATION S7 SYSTEM
FDA Adverse Event
Malfunction
·MEDTRONIC NAVIGATION, INC.·Product code HAW·December 20, 2012
15.0MM REAMER HEAD FOR RIA 2 STERILE
FDA Adverse Event
Malfunction
·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HRX·June 21, 2021