7 results
·
26ms
·
Sources: EU EUDAMED, US FDA
CLIRANS TE12 HOLLOW FIBER DIALYZER
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
DYNAPULSE 500G (DP500G) BLLOD PRESSURE MONITORING SYSTEM
FDA 510(k)
FDA Class 2
·Cardiovascular
Advanced Skin Renewing Device
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
PEEL-AWAY INTRODUCER KIT 7F, .038, 14CM SHEATH
FDA Adverse Event
Injury
·ST. JUDE MEDICAL, INC. (AF-MINNETONKA)·Product code DQX·May 5, 2014
EXTERNAL PULSE GENERATOR
FDA Adverse Event
Malfunction
·MEDTRONIC MILACA INC.·Product code DTE·October 31, 2012
ACTIVA PC
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code MHY·August 16, 2010
Philips Zenition 70, Model Number: 718133
FDA Enforcement
Class II
·Ongoing·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·November 20, 2024