25 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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CRE BALLOON DILATATION CATHETER
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
JOBST SensiFoot
FDA UDI
BSN MEDICAL, INC.·00035664108335·SENSIFOOT 8-15 MM HG KNEE HIGH LARGE WHITE 1 EN...
Marina Medical
FDA UDI
MARINA MEDICAL INSTRUMENTS, INC.·00840306818837·Kelly Retractor, 1-3/4" x 6"
AT WORK DRUG TEST, MODEL 9177T AWT
FDA 510(k)
FDA Class 2
·Clinical Toxicology
SYLE SMARTIP
FDA 510(k)
FDA Class 1
·Dental
PRISMAFLEX
FDA Adverse Event
Injury
·GAMBRO LUNDIA AB·Product code KDI·February 6, 2014
PRISMAFLEX
FDA Adverse Event
Death
·GAMBRO LUNDIA AB·Product code KDI·April 11, 2014
PRISMAFLEX
FDA Adverse Event
Injury
·GAMBRO LUNDIA AB·Product code KDI·November 2, 2012
PRISMAFLEX
FDA Adverse Event
Injury
·GAMBRO LUNDIA AB·Product code KDI·February 15, 2012
PRISMAFLEX
FDA Adverse Event
Injury
·GAMBRO LUNDIA AB·Product code KDI·December 23, 2013
QUATTRODE
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·May 9, 2013
UNKNOWN KNEE
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JWH·September 23, 2014
SYNCHRON® URIC ACID REAGENT
FDA Adverse Event
Malfunction
·BECKMAN COULTER INC.·Product code KNK·June 1, 2011
PRISMAFLEX
FDA Adverse Event
Injury
·GAMBRO LUNDIA AB·Product code KDI·February 6, 2014
PRISMAFLEX
FDA Adverse Event
Death
·GAMBRO LUNDIA AB·Product code KDI·January 10, 2014
PRISMAFLEX
FDA Adverse Event
Death
·GAMBRO LUNDIA AB·Product code KDI·January 3, 2014
PRISMAFLEX
FDA Adverse Event
GAMBRO LUNDIA AB·Product code KDI·February 6, 2014
PRISMAFLEX
FDA Adverse Event
Injury
·GAMBRO LUNDIA AB·Product code KDI·August 13, 2012
PRISMAFLEX
FDA Adverse Event
Injury
·GAMBRO LUNDIA AB·Product code KDI·January 10, 2014
PANEL PHOENIX NMIC/ID-308
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code LON·March 14, 2023