8 results
·
19ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
TEMPO 4 ANGIOGRAPHY CATHETER (VARIOUS)
FDA 510(k)
FDA Class 2
·Cardiovascular
LateralALIF
FDA UDI
Nuvasive, Inc.·00887517840080·ALIF Pin, 60mm Anchoring
EARPOPPER, MODEL EP-2000, EP-2100, EP-3000
FDA 510(k)
FDA Unclassified
·Unknown
TURBOX
FDA 510(k)
FDA Class 1
·Immunology
RIATA ST ACTIVE FIXATION
FDA Adverse Event
Malfunction
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·February 21, 2013
HOMECHOICE CYCLER-REFURBISHED
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - LARGO·Product code FKX·January 30, 2011
TISSUE RETRIEVAL SYSTEM
FDA Adverse Event
Malfunction
·ANCHOR PRODUCTS CO.·Product code GCJ·July 8, 2014
DISC RONGEUR STRAIGHT WITHOUT TEETH 6MM WIDTH 330MM
FDA Adverse Event
Malfunction
·SYNTHES TUTTLINGEN·Product code HTX·April 27, 2016