8 results
·
18ms
·
Sources: EU EUDAMED, US FDA
SUNBEAM EVAPORATIVE HUMIDIFIER 663 & 664
FDA 510(k)
FDA Class 1
·Anesthesiology
APEX Knee System
FDA UDI
Omni Life Science, Inc.·00841690192312·Revision Knee Reamer Spiral Fluted - Zimmer 22mm
Dunamis Interference Screw
FDA 510(k)
FDA Class 2
·Orthopedic
REPROCESSED DEFLECTABLE ELECTROPHYSIOLOGY DIAGNOSTIC CATHETERS
FDA 510(k)
FDA Class 2
·Cardiovascular
CADD-SOLIS VIP AMBULATORY INFUSION PUMP
FDA Adverse Event
Malfunction
·ICU MEDICAL, INC.·Product code FRN·June 24, 2025
DA VINCI ROBOT
FDA Adverse Event
Injury
·Product code NAY·May 30, 2014
INSIGNIA
FDA Adverse Event
Injury
·GUIDANT CRM CLONMEL IRELAND·Product code LWP·October 4, 2010
UNKNOWN DEPUY LCS FEMORAL COMPONENT
FDA Adverse Event
Injury
·DEPUY WARSAW·Product code JDI·November 29, 2012