6 results
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27ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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EXTREMITY BONE SCREW
FDA 510(k)
FDA Class 2
·Orthopedic
FLEX Microwave Ablation System and Accessories
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
BARD BALLOON DILATION KIT WITH TRIFUNNEL GASTROSTOMY TUBE
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
9800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 19, 2014
ORTHO SUMMIT SAMPLE HANDLING SYSTEM
FDA Adverse Event
Malfunction
·HAMILTON BONADUZ AG·Product code MMH·February 15, 2013
INFUSOR LV5, 12 PK
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - IRVINE·Product code MEB·January 18, 2011