7 results
·
17ms
·
Sources: EU EUDAMED, US FDA
PULMANEX TM (MODIFICATION)
FDA 510(k)
FDA Class 2
·Anesthesiology
Arthrex®
FDA UDI
ARTHREX, INC.·00888867125797·HEADLESS COMPRES SCRW 3.0X26MM
Ultra/Phonic Scanning Gel
FDA 510(k)
FDA Class 2
·Radiology
OK METER BLOOD GLUCOSE MONITORING SYSTEM
FDA 510(k)
FDA Class 2
·Clinical Chemistry
CEMENTED HUMERAL STEM 6.5
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code KWS·June 6, 2014
ZEPHYR XL DR
FDA Adverse Event
Death
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWP·December 10, 2012
SPRINT FIDELIS
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO, INC.·Product code LWS·October 9, 2010