6 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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VIBRONICS AUTO CORE BIOPSY DEVICE (ACBD)
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
OLYMPIC BILI-LITE-PAD(TM)
FDA 510(k)
FDA Class 2
·General Hospital
G.E. DXS 350/550/650/650II SINGLE PHASE GENERATORS
FDA 510(k)
FDA Class 1
·Radiology
ACTIVE FIXATION ENDOCARDIAL LEAD
FDA Adverse Event
Injury
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DTB·January 9, 2013
PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM
FDA Adverse Event
Injury
·AV-REDWOOD CITY·Product code MGB·November 22, 2010
PINN MAR NEUT 28IDX54OD
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.·Product code LPH·July 1, 2014