8 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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KARL STORZ ELECTRONIC LAPAROFLATOR
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
SwishTapered™ Implant
FDA UDI
IMPLANT DIRECT SYBRON MANUFACTURING LLC·10841307106425·4.1mmD x 14mmL, 4.8mmD Platform
De Soutter Medical
FDA UDI
DE SOUTTER MEDICAL LIMITED·05051471150720·K-WIRE - SINGLE TROCAR 1.1mm DIA x 100mm
CUTIVA(TM) Topical Skin Adhesive (RM-1700); CUTIVA(TM) PLUS Skin Closure System (RM-1739)
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
ANATECH X-RAY GENERATOR
FDA 510(k)
FDA Class 1
·Radiology
PELORIS RAPID TISSUE PROCESSOR
FDA Adverse Event
Malfunction
·LEICA BIOSYSTEMS MELBOURNE·Product code IEO·January 4, 2013
SPECTRUM INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code FRN·February 3, 2014
ANIMAS INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·ANIMAS CORP.·Product code LZG·December 2, 2010