13 results
·
23ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
FLEXISCOPE II ARTHROSCOPES AND ACCESSORIES
FDA 510(k)
FDA Class 2
·Orthopedic
Instrument Case
FDA UDI
KATENA PRODUCTS, INC.·00841668110997·DOUBLE PLASTIC STERILIZATION CASE
PICCOLO BASIC METABOLIC PANEL
FDA Adverse Event
Malfunction
·ABAXIS, INC.·Product code CGX·October 22, 2020
PICCOLO COMPREHENSIVE METABOLIC PANEL
FDA Adverse Event
Malfunction
·ABAXIS, INC.·Product code CGX·November 3, 2020
Vu aPod™ - L
FDA UDI
Seaspine Orthopedics Corporation·10889981118051·Wide Standard Implant Caddy, 40mm
AVIEW Modeler
FDA 510(k)
FDA Class 2
·Radiology
PHEROCIOUS 10.5 FR (24 CM, 28 CM AND 32 CM), MODELS 430102440, 430102840, 430103240
FDA 510(k)
FDA Class 2
·General Hospital
EARIGATOR
FDA Adverse Event
Malfunction
·SURYA TECHNOLOGIES INTERNATIONAL·Product code JYH·January 4, 2001
ACCU-CHEK ® INFORM METER
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code NBW·March 7, 2013
SPRINT QUATTRO SECURE
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO, INC.·Product code LWS·February 15, 2011
SPRINT QUATTRO SECURE
FDA Adverse Event
Injury
·MPRI·Product code LWS·August 8, 2014
TAXUS EXPRESS2 PACLITAXEL-ELUTING CORONARY STENT SYSTEM
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORP.·Product code NIQ·May 3, 2007
TAXUS EXPRESS2 PACLITAXEL-ELUTING CORONARY STENT SYSTEM
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC·Product code NIQ·May 3, 2007