8 results
·
24ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
MEDAJET XL - JET INJECTOR
FDA 510(k)
FDA Class 2
·General Hospital
PRECIMED CANNULATED SCREW SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
ARGOS
FDA 510(k)
FDA Class 2
·Ophthalmic
THUNDERBEAT 5 MM, 35 CM, FRONT-ACTUATED GRIP TYPE S
FDA Adverse Event
Malfunction
·OLYMPUS MEDICAL SYSTEMS CORP.·Product code GEI·October 9, 2019
ABX MINOTROL 16
FDA Adverse Event
Other
·HORIBA MEDICAL·Product code GKZ·June 6, 2013
EDWARDS MC3 TRICUSPID ANNULOPLASTY SYSTEM
FDA Adverse Event
Death
·EDWARDS LIFESCIENCES·Product code KRH·October 2, 2010
MICRO-LINE STRAIGHT HDPC 1:1 F/2. 35X70MM
FDA Adverse Event
Malfunction
·AESCULAP AG & CO. KG·Product code HWE·March 20, 2014
REPLY
FDA Adverse Event
Injury
·SORIN CRM S.R.L.·Product code NVZ·November 23, 2012