10 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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MGD-3
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
THD disposable sterile and not sterie Ano-, Procto- Rectoscopes and Light-scope
FDA UDI
THD SPA·08033737710418·The THD Light-Scope rectoscope is a disposable ...
Pilot Spinal System
FDA UDI
Life Spine, Inc.·00190837009663·
OLYMPUS SONOSURG TROCAR XT3900 SYSTEM
FDA 510(k)
FDA Unclassified
·Unknown
CORAMATE/SPIROTOME SYSTEM
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
N/A
FDA UDI
Zimmer, Inc.·00889024064805·
SUPERION INDIRECT DECOMPRESSION SYSTEM
FDA Adverse Event
Injury
·VERTIFLEX INC.·Product code NQO·June 11, 2020
SPECTRUM INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code FRN·January 8, 2014
TREK CORONARY DILATATION CATHETER
FDA Adverse Event
Malfunction
·AV-TEMECULA-CT·Product code LOX·October 22, 2012
840 VENTILATOR
FDA Adverse Event
Malfunction
·PURITAN BENNETT CORP·Product code CBK·August 10, 2010