7 results
·
24ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
NuVasive MOD-EX XLIF Interbody System, NuVasive MOD-EX XLIF Plated 2.0 Interbody System
FDA 510(k)
FDA Class 2
·Orthopedic
Blade Scalpel
FDA UDI
KATENA PRODUCTS, INC.·00841668113547·SLIT BLADE 3.2MM ANGLED (BX/5)
Captivator Single-Use Polypectomy Snares, Captiflex Single-Use Polypectomy Snares
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
ELECTROMEDICARIN 900
FDA 510(k)
FDA Class 2
·Physical Medicine
ACCU-CHEK COMPACT TEST DRUM
FDA Adverse Event
Injury
·ROCHE DIAGNOSTICS·Product code LFR·November 4, 2008
TOTALCARE
FDA Adverse Event
Malfunction
·HILL-ROM INC.·Product code FNL·July 18, 2011
OT VERIO PRO PLUS METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 11, 2013