9 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Carecube Negative Pressure Isolation Chamber
FDA 510(k)
FDA Class 2
·General Hospital
Rx Knee Tibial Cone Augment Reamer Size Large Stacked
FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215147877·
XSIF-1TQ140A SMALL INTESTINAL VIDEOSCOPE
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
Procise CRP, ProciseDx Analyzer, ProciseDx Calibration Cartridge
FDA 510(k)
FDA Class 2
·Immunology
BD INTIMA-II Y 24GAX0.75IN PRN/EC SLM
FDA Adverse Event
Malfunction
·BECTON DICKINSON MEDICAL DEVICES CO., LTD. SUZHOU·Product code FOZ·November 22, 2021
BD INTIMA-II CLOSED IV CATHETER SYSTEM
FDA Adverse Event
Malfunction
·BD (SUZHOU)·Product code FOZ·February 12, 2021
MICRO RECIPROCATING SAW
FDA Adverse Event
Malfunction
·STRYKER INSTRUMENTS KALAMAZOO·Product code ERL·July 25, 2011
GE OEC 9900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·November 13, 2008
BHR
FDA Adverse Event
Injury
·SMITH & NEPHEW ORTHOPAEDICS LTD·Product code NXT·July 17, 2013