9 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Intrauterine Access Balloon Catheter, Selective Salpingography Catheter
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
INTRAUTERINE ACCESS BALLOON CATHETER
FDA Adverse Event
Malfunction
·COOK INC·Product code LKF·December 10, 2020
SELECTIVE SALPINGOGRAPHY CATHETER
FDA Adverse Event
Malfunction
·COOK INC·Product code LKF·November 19, 2021
BLACK WIDOW ANTERIOR BUTTRESS PLATE
FDA 510(k)
FDA Class 2
·Orthopedic
HEADSTAR MEDICAL SMALL VOLUME JET NEBULIZER
FDA 510(k)
FDA Class 2
·Anesthesiology
STELO GLUCOSE BIOSENSOR SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code SAF·July 12, 2025
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·June 21, 2013
CARPENTIER-EDWARDS PERIMOUNT PLUS PERICARDIAL BIOPROSTHESIS
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code DYE·July 27, 2011
SOLETRA
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code MHY·September 30, 2008