28 results
·
22ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
VR MEDICAL ENTERAL ORAL SYRINGE
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
JOBST SensiFoot
FDA UDI
BSN MEDICAL, INC.·00035664108533·SENSIFOOT 8-15 MM HG CREW LARGE BLACK 1 EN FR ES
Marina Medical
FDA UDI
MARINA MEDICAL INSTRUMENTS, INC.·00840306819049·Walther-Simpson Malleable Retractor, 3.8 X 10cm...
Cosmolock
FDA UDI
Kalitec Direct LLC·B07311K1100530·Caddie, 7.5mm Screws
6MM BD¿ INSULIN SYRINGE
FDA Adverse Event
Malfunction
·BD MEDICAL - DIABETES CARE·Product code FMF·August 21, 2017
COBAS 8000 MODULAR SERIES ANALYZER
FDA 510(k)
FDA Class 2
·Immunology
GUIDER SOFTIP GUIDING CATHETER XF 5F
FDA 510(k)
FDA Class 2
·Cardiovascular
General Instrument
FDA UDI
ALPHATEC SPINE, INC.·00840180511640·3mm Up-biting Toothed Pituitary, 8"
General Instrument
FDA UDI
ALPHATEC SPINE, INC.·00840180511626·3mm Straight Toothed Pituitary, 8"
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·May 7, 2025
DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·September 29, 2020
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
FOLFUSOR
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - IRVINE·Product code MEB·June 2, 2011
UPHOLD VAGINAL SUPPORT SYSTEM
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·May 14, 2013
SYSTEM, PERITONEAL, AUTOMATIC DELIVERY
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·September 23, 2014
PRISMAFLEX
FDA Adverse Event
Injury
·GAMBRO LUNDIA AB·Product code KDI·February 6, 2014