8 results
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27ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
Y CONNECTOR
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
NON-BR2000 LARGE BONE BLADES
FDA UDI
Peter Brasseler Holdings, LLC·00887919095194·KM519-21
BlueRay3
FDA UDI
AMERICAN ORTHODONTICS CORPORATION·00190746007897·BLUE RAY MINI LED HAND PIECE
THE EDGE DETECTOR, MODEL 1118
FDA 510(k)
FDA Class 2
·Radiology
STERISPINE PS
FDA 510(k)
FDA Class 2
·Orthopedic
HOMECHOICE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - LARGO·Product code FKX·June 5, 2014
FINELINE II
FDA Adverse Event
Malfunction
·CPI - DEL CARIBE·Product code NVN·October 4, 2010
NON AC-POWERED PATIENT LIFT
FDA Adverse Event
Malfunction
·INVACARE SUZHOU·Product code FSA·November 29, 2012