9 results
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28ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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HERMLE Z230H
FDA 510(k)
FDA Class 2
·Hematology
Instrument Case
FDA UDI
KATENA PRODUCTS, INC.·00841668110942·STERILIZING CASE PLASTIC SMALL
EASYTOUCH
FDA Adverse Event
Malfunction
·BERPU MEDICAL TECHNOLOGY CO., LTD·Product code FMF·November 20, 2023
VISIA
FDA 510(k)
FDA Class 2
·Radiology
Mobility Scooter, Model W3468
FDA 510(k)
FDA Class 2
·Physical Medicine
I-STAT 6+ CARTRIDGE
FDA Adverse Event
Malfunction
·ABBOTT POINT OF CARE·Product code JGS·December 8, 2020
LIGASURE
FDA Adverse Event
Malfunction
·COVIDIEN VALLYELAB·Product code GEI·November 12, 2010
LASSO® 2515 NAV ECO VARIABLE CATHETER
FDA Adverse Event
Malfunction
·BIOSENSE WEBSTER, INC. (JUAREZ)·Product code DRF·July 8, 2014
AUTOPULSE LI-ION BATTERY
FDA Adverse Event
Malfunction
·ZOLL CIRCULATION, INC.·Product code DRM·December 17, 2012