8 results
·
19ms
·
Sources: EU EUDAMED, US FDA
CLYDE CORONARY GUIDEWIRE
FDA 510(k)
FDA Class 2
·Cardiovascular
artegral
FDA UDI
Merz Dental GmbH·D7091970528·anteriors; shade BL3; mould BS
Sklar
FDA UDI
SKLAR CORPORATION·10649111335877·CURETTE EXCA W/HOLE 2.5MM
PHILIPS ESSENTA DR
FDA 510(k)
FDA Class 2
·Radiology
Sterispine PS
FDA 510(k)
FDA Class 2
·Orthopedic
LIFEVEST WCD 4000 SYSTEM
FDA Adverse Event
Malfunction
·ZOLL LIFECOR CORPORATION·Product code MVK·June 10, 2014
RESERVOIR 1.8ML
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code FRN·February 20, 2013
UNKNOWN DEPUY ASR XL ACETABULAR SYSTEM
FDA Adverse Event
Injury
·DEPUY IINTL, LTD.·Product code KWA·January 20, 2011