12 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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NAVARRE LOCKING PIGTAIL UNIVERSAL DRAINAGE CATHETER
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
Millennium
FDA UDI
Avalign Technologies, Inc.·00190776094973·Frazier Suction Tube, RoundSlot
LGN PS HIGH FLEX XLPE SZ 1-2 13MM
FDA Adverse Event
Injury
·SMITH & NEPHEW, INC.·Product code JWH·August 9, 2017
GII PS HI FLEX ISRT SZ 7-8 9
FDA Adverse Event
Injury
·SMITH & NEPHEW, INC.·Product code JWH·July 19, 2017
Cable-Ready® Cable Grip System: Cable-Ready® GTR System, Cable-Ready® 1.8mm Cerclage Cables
FDA 510(k)
FDA Class 2
·Orthopedic
INNOCOR
FDA 510(k)
FDA Class 2
·Cardiovascular
LGN PS HIGH FLEX XLPE SZ 1-2 13MM
FDA Adverse Event
Injury
·SMITH & NEPHEW, INC.·Product code JWH·August 9, 2017
GII ARTICULAR INSERTER/EXTRACT
FDA Adverse Event
Injury
·SMITH & NEPHEW, INC.·Product code MBH·February 9, 2018
DRUG ELUTING PERMANENT RIGHT VENTRICULAR (RV) OR RIGHT ATRIAL (RA) PACEMAKER ELE
FDA Adverse Event
Injury
·MPRI·Product code NVN·February 9, 2013
EASYTRAK 2
FDA Adverse Event
Injury
·CPI - DEL CARIBE·Product code OJX·January 7, 2011
EGIA ULTRA UNIVERSAL STAPLER
FDA Adverse Event
Malfunction
·COVIDIEN·Product code GDW·July 11, 2014
NONE
FDA Adverse Event
Death
·GUIDANT CORPORATION·Product code LWS·March 18, 2010