8 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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R&D BATTERIES, PART NOS. 5243, 5104, AND 5481
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Omnisorb
FDA UDI
TIDI PRODUCTS, LLC·00618125106028·Nonwoven Sponges, Open Weave, 4 Ply
HOVEROUND POWER WHEELCHAIR, MODEL HD700
FDA 510(k)
FDA Class 2
·Physical Medicine
VERIGENE ENTERIC PATHOGEN NUCLEIC ACID TEST (EP)
FDA 510(k)
FDA Class 2
·Microbiology
BD SEDI-40
FDA Adverse Event
Malfunction
·BECTON DICKINSON·Product code JKA·March 17, 2022
PRIMEADVANCED
FDA Adverse Event
Malfunction
·MDT PUERTO RICO OPERATIONS CO·Product code LGW·February 4, 2013
MERIT CUSTOM KIT
FDA Adverse Event
Malfunction
·MERIT MEDICAL SYSTEMS, INC.·Product code DQO·November 9, 2010
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·July 17, 2014