8 results
·
25ms
·
Sources: EU EUDAMED, US FDA
VTI DISPOSABLE PRESSURE DISPLAY SET
FDA 510(k)
FDA Class 2
·Cardiovascular
STERN ERA IMPLANT ABUTMENT
FDA 510(k)
FDA Class 2
·Dental
EMIT (R) II CALIBRATOR A LEVEL 1 (CUTOFF) 2 (HIGH)
FDA 510(k)
FDA Class 2
·Clinical Toxicology
FRESENIUS DIALYSIS DELIVERY SYSTEM
FDA Adverse Event
Malfunction
·FRESENIUS MEDICAL CARE-NORTH AMERICA·Product code KDI·May 16, 2008
PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)
FDA Adverse Event
Malfunction
·INVACARE FLORIDA OPERATIONS·Product code CAW·February 5, 2013
SIEMENS BRAND NAME: ARTISTE MV
FDA Adverse Event
Malfunction
·SIEMENS MEDICAL SOLUTIONS USA, INC.·Product code IYE·December 10, 2010
PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)
FDA Adverse Event
Malfunction
·INVACARE FLORIDA OPERATIONS·Product code CAW·July 18, 2014
SINGLE USE PAPER FILTER WITH INDICATOR
FDA Adverse Event
Malfunction
·AESCULAP AG·Product code FRG·January 30, 2019