7 results
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27ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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MITEK QUICKANCHOR(TM), MODIFICATION
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
FAC-5 - Kent Class B
FDA UDI
Certified Safety Manufacturing, Inc.·00766588150895·FAC-5 - Kent Class B
MEGA LUMBAR PUNCTURE KIT
FDA 510(k)
FDA Class 2
·General Hospital
ABUSCREEN FP FOR CANNABINOIDS (50-100)
FDA 510(k)
FDA Class 2
·Clinical Toxicology
PRIME 5TH WHEEL STRETCHER, 30"
FDA Adverse Event
Malfunction
·STRYKER MEDICAL·Product code FPO·December 7, 2012
TERUMO CDI 500 BLOOD PARAMETER MONITOR
FDA Adverse Event
Malfunction
·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DRY·November 17, 2010
MECHANICAL (MANUAL) WHEELCHAIR
FDA Adverse Event
Malfunction
·INVAMEX·Product code IOR·July 7, 2014