8 results
·
23ms
·
Sources: EU EUDAMED, US FDA
Ready to use Nelaton Catheter
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
MEE-1000A NEUROMASTER
FDA 510(k)
FDA Class 2
·Neurology
VariAx 2 Wrist Fusion System
FDA 510(k)
FDA Class 2
·Orthopedic
ILAB POLARIS MULTI-MODALITY GUIDANCE SYSTEM
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code DQK·March 3, 2025
ILAB? POLARIS MULTI-MODALITY GUIDANCE SYSTEM
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code DQK·May 14, 2026
ACUITY CENTRAL MONITORING
FDA Adverse Event
Malfunction
·WELCH ALLYN PROTOCOL, INC.·Product code DSI·August 10, 2011
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·November 14, 2014
DEPTH GAUGE F/SCR Ø2+2.4 MEAS-RANGE UP-T
FDA Adverse Event
Malfunction
·SYNTHES GMBH·Product code HTJ·July 29, 2013