10 results
·
21ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
MITYVAC
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
Para-Pak Ultra SAF
FDA UDI
MERIDIAN BIOSCIENCE, INC.·00840733102851·The Para-Pak Ultra SAF is a convenient system f...
Para-Pak Ultra SAF
FDA UDI
MERIDIAN BIOSCIENCE, INC.·00840733102455·The Para-Pak Ultra SAF is a convenient system f...
APC/Fire™ 750 anti-human CD20
FDA UDI
BIOLEGEND, INC.·00810034702722·URL: https://www.biolegend.com/en-us/products/a...
TSRH H/M HOOK HOLDER W/ROD MOVER
FDA 510(k)
FDA Class 2
·Orthopedic
MEDELA THOPAZ, MODEL 200 0288
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
ARCHITECT I2000SR ANALYZER
FDA Adverse Event
Malfunction
·ABBOTT MANUFACTURING, INC.·Product code JJE·June 16, 2009
HYPODERMIC NEEDLE-PRO AND NEEDLE WITH NEEDLE PROTECTION DEVICE
FDA Adverse Event
Malfunction
·SMITHS MEDICAL ASD, INC.·Product code FMJ·February 1, 2013
RENAL - DISPOSABLE
FDA Adverse Event
Injury
·Product code KDJ·February 7, 2011
4.5 MICROEZ UNIVERSAL PTFE MICROINTRO SAFETY KIT
FDA Adverse Event
Malfunction
·BARD ACCESS SYSTEMS INC.·Product code DYB·July 2, 2014