6 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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3000 ELECTRONIC INSUFFLATOR MODIFICATION
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
CULTROL-ANTIBIOTIC/ANTIMYCOTIC SOLUT
FDA 510(k)
FDA Class 1
·Microbiology
APRO 55 Catheter
FDA 510(k)
FDA Class 2
·Cardiovascular
ANIMAS INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·ANIMAS CORP.·Product code LZG·December 2, 2010
SPECTRUM INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code FRN·February 3, 2014
AUTOPULSE NIMH BATTERY
FDA Adverse Event
Malfunction
·ZOLL CIRCULATION, INC.·Product code DRM·December 21, 2012