8 results
·
28ms
·
Sources: EU EUDAMED, US FDA
Numen Helia Coil Embolization System; NumenFR Detachment System
FDA 510(k)
FDA Class 2
·Neurology
MSI Precision Specialty Instruments
FDA UDI
Med Saver, Inc.·00194613018030·K-Wire, Single Ended, Trocar Point, Diameter Si...
CX50N, CX50YQS
FDA 510(k)
FDA Class 2
·Radiology
MEDTOX OXYCODONE
FDA 510(k)
FDA Class 2
·Clinical Toxicology
UNICEL DXC 600I SYNCHRON ACCESS CLINICAL SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER·Product code JJE·November 18, 2014
ASR UNI FEMORAL IMPL SIZE 43
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL·Product code KWA·September 22, 2011
FLANGE FIXTURE AND ABUTMENT
FDA Adverse Event
Injury
·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code LXB·August 1, 2013
RADIESSE (+) INJECTABLE IMPLANT
FDA Adverse Event
Injury
·MERZ NORTH AMERICA, INC.·Product code LMH·April 7, 2021