10 results
·
29ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
CADD-LEGACY PCA AMBULATORY INFUSION SYSTEM, MODEL 6300
FDA 510(k)
FDA Class 2
·General Hospital
CADD-LEGACY® PCA AMBULATORY INFUSION PUMP
FDA Adverse Event
Injury
·SMITHS MEDICAL ASD INC.,·Product code MEA·March 29, 2016
CIRCUITGUARD CIRCUITGUARD HME
FDA Adverse Event
Other
·ARC MEDICAL INC., ANESTHESIA & RESPIRATORY CARE·Product code BYD·July 20, 2005
DISTAL RADIO-ULNAR JOINT IMPLANT
FDA 510(k)
FDA Class 2
·Orthopedic
Lifetech Cardio Model 8301 Temporary Pacemaker
FDA 510(k)
FDA Class 2
·Cardiovascular
CADD LEGACY PLUS PUMP
FDA Adverse Event
Malfunction
·SMITHS MEDICAL ASD, INC.·Product code FRN·January 20, 2025
CADD LEGACY PLUS PUMP
FDA Adverse Event
Malfunction
·ST PAUL·Product code FRN·September 9, 2022
HEARTSTART XL+DEFIB/MONITOR
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS·Product code MKJ·June 13, 2014
POSEY KEEPSAFE DELUXE
FDA Adverse Event
Malfunction
·J. T. POSEY CO.·Product code KMI·January 31, 2013
ROTABLATOR ROTATIONAL ATHERECTOMY SYSTEM
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - CORK·Product code MCX·February 9, 2011