8 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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AP50/30 Insufflator with Insuflow Port
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
GUIDED MEASUREMENT CATHETER (GMC)
FDA 510(k)
FDA Class 2
·Cardiovascular
EVIS EXERA III VIDEO SYSTEM
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
AZUR VASCULAR PLUG 8
FDA Adverse Event
Injury
·MICROVENTION, INC.·Product code KRD·March 29, 2022
EVIS EXERA III GASTROINTESTINAL VIDEOSCOPE
FDA Adverse Event
Malfunction
·AIZU OLYMPUS CO., LTD.·Product code FDS·July 22, 2022
PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·June 26, 2013
TENDRIL ST
FDA Adverse Event
Injury
·ST. JUDE MEDICAL, CRMD·Product code NVN·January 13, 2014
E SERIES DEFIBRILLATOR
FDA Adverse Event
Malfunction
·ZOLL MEDICAL CORPORATION·Product code MKJ·July 28, 2011