25 results · 23ms · Sources: EU EUDAMED, 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