8 results
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23ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
MERIDIAN MEDICAL SYSTEMS BREATHING FILTER
FDA 510(k)
FDA Class 2
·Anesthesiology
N/A
FDA UDI
Tyber Medical, LLC·M695M9252170·
FORMASURE TEST REAGENT
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
MAX-E-VAC
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
STORZ
FDA Adverse Event
Malfunction
·KARL STORZ ENDOSCOPY-AMERICA, INC.·Product code FJL·June 12, 2014
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·January 22, 2013
ENTRUST AT
FDA Adverse Event
Injury
·MEDTRONIC MED REL, INC.·Product code LWS·December 14, 2010
MENTOR MEMORYGEL BREAST IMPLANT
FDA Adverse Event
Injury
·MENTOR TEXAS·Product code FTR·April 29, 2020