7 results
·
27ms
·
Sources: EU EUDAMED, US FDA
AMB-ALERT
FDA 510(k)
FDA Class 1
·General Hospital
DeRoyal
FDA UDI
DEROYAL INDUSTRIES, INC.·00749756394000·NEURO BASIC PACK
K-ASSAY HS-CRP CONTROLS
FDA 510(k)
FDA Class 2
·Immunology
SYNGO.VIA WEB VIEWER
FDA 510(k)
FDA Class 2
·Radiology
LRG TAP PRI MOD NCK 0DEG 38MM
FDA Adverse Event
Injury
·STRYKER ORTHOPAEDICS CORK·Product code MEH·January 4, 2013
LIGACLIP MCA
FDA Adverse Event
Malfunction
·ETHICON ENDO SURGERY·Product code FZP·November 1, 2010
RIATA ACTIVE FIXATION
FDA Adverse Event
Injury
·ST. JUDE MEDICAL, INC., CRMD·Product code NVY·July 2, 2014