7 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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WALLACH LEEP PROCEDURE KIT
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
BOSS Instruments
FDA UDI
BOSS INSTRUMENTS, LTD., INC.·00888515243514·Micro Rotating Backbiter, ped
SMT-50X
FDA 510(k)
FDA Class 2
·Radiology
FRESENIUS PD+ EXCHANGE DEVICE
FDA 510(k)
FDA Class 1
·Dental
E SERIES DEFIBRILLATION
FDA Adverse Event
Malfunction
·ZOLL MEDICAL CORP·Product code MKJ·December 14, 2010
ASR ACETABULAR CUPS 62
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL·Product code KWA·January 30, 2013
SPECTRUM INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORP·Product code FRN·February 3, 2014