7 results
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18ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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MENTOR(R) WET-FIELD(R) II AC COAGULATOR, 22-1305
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
M2A MAGNUM PF CUP
FDA Adverse Event
Malfunction
·BIOMET·Product code KWA·March 21, 2011
E-Z EM PERCUPUMP 2001 CT INJECTOR
FDA 510(k)
FDA Class 2
·Radiology
INTRICON DATRIX CENTAURI MT AMBULATORY PATIENT ECG TELEMETRY SYSTEM (APETS)
FDA 510(k)
FDA Class 2
·Cardiovascular
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·July 13, 2015
COGNIS
FDA Adverse Event
Injury
·GUIDANT CRM CLONMEL IRELAND·Product code NIK·January 11, 2013
RENAL - DISPOSABLE
FDA Adverse Event
Injury
·Product code KDJ·November 30, 2010