8 results
·
24ms
·
Sources: EU EUDAMED, US FDA
KEELER ACU 22XT OPHTHALMIC CRYO UNIT
FDA 510(k)
FDA Class 2
·Ophthalmic
GC Initial™
FDA UDI
Gc America Inc.·J0228745551·GC Initial™ Ti Dentin DA4, 50g
BEAR VENTI--VOICE
FDA 510(k)
FDA Class 1
·Ear, Nose, Throat
PATHFINDER CARDIOVASCULAR CATHETER
FDA 510(k)
FDA Class 2
·Cardiovascular
BRIVO 785
FDA Adverse Event
Malfunction
·GE HANGWEI MEDICAL SYSTEMS CO.·Product code JAA·April 22, 2014
MAXIMO VR
FDA Adverse Event
Injury
·MEDTRONIC S.A.·Product code LWS·October 19, 2010
AC-POWERED ADJUSTABLE HOSPITAL BED, INCLUDING RAILS
FDA Adverse Event
Malfunction
·INVACARE FLORIDA OPERATIONS·Product code FNL·December 14, 2012
OSTYCUT BONE BIOPSY NEEDLE
FDA Adverse Event
Injury
·ANGIOMED GMBH & CO. MEDIZINTECHNIK KG·Product code DWO·September 7, 2015