7 results
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26ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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E7512 PREMIE REM POLYHESIVE II PATIENT RETURN ELECTRODE
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
PANOSOL II UAB-228
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
HEARING AID (IN-THE-EAR)
FDA 510(k)
FDA Class 1
·Ear, Nose, Throat
UNKNOWN DRILL BIT
FDA Adverse Event
Malfunction
·ZIMMER BIOMET, INC.·Product code LXH·January 7, 2025
DIMENSION VISTA® CLINICAL CHEMISTRY SYSTEM
FDA Adverse Event
Malfunction
·SIEMENS HEALTHCARE DIAGNOSTICS INC - GLASGOW·Product code KXT·March 8, 2013
HYDROGEL COATED PERCUFLEX(R) DRAINAGE CATHETERS
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - SPENCER·Product code FGE·February 17, 2011
NAVISTAR® THERMOCOOL®
FDA Adverse Event
Injury
·BIOSENSE WEBSTER, INC (IRWINDALE)·Product code OAD·August 8, 2014