6 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ERBOTOM ICC 50
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
REUSABLE LIQUIDPROOF BOOTIE
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
ABDOMINAL / THORACIC PATIENT DRAPE
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
AUTOPULSE NIMH BATTERY
FDA Adverse Event
Malfunction
·ZOLL CIRCULATION INC·Product code DRM·January 2, 2013
FUSION OMNI-TOME PRE-LOADED SPHINCTEROTOME
FDA Adverse Event
Malfunction
·COOK ENDOSCOPY·Product code KNS·December 3, 2010
HEARTWARE® VENTRICULAR ASSIST SYSTEM
FDA Adverse Event
Injury
·HEARTWARE, INC·Product code DSQ·July 15, 2014