11 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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DIAMEDIX IS-MEASLES IGG TEST SYSTEM
FDA 510(k)
FDA Class 1
·Microbiology
BD PYXIS¿ MEDSTATION¿ ES
FDA Adverse Event
Malfunction
·CAREFUSION 303, INC.·Product code BRY·March 31, 2025
CMI VACUUM PUMP
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
ENVISAN PAD
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
PSO KNEE BONE SUBSTITUTION
FDA Adverse Event
Injury
·BIOMET SPAIN, S.L.·Product code KRO·April 22, 2022
1.5MM RESORB ORBITAL FLOOR PL 24MMX24MM W/BENDING TEMP-STER
FDA Adverse Event
Injury
·SYNTHES USA·Product code JEY·November 2, 2012
PSO KNEE BONE SUBSTITUTION
FDA Adverse Event
Injury
·BIOMET SPAIN, S.L.·Product code KRO·July 18, 2019
VERSACARE BED
FDA Adverse Event
Malfunction
·HILL-ROM, INC.·Product code FNL·January 4, 2013
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·August 3, 2014
*
FDA Adverse Event
Malfunction
·BARD·Product code KOD·January 21, 2011
UNKNOWN HEAD
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWA·February 16, 2018