9 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Cocoon Convective Warming System
FDA 510(k)
FDA Class 2
·Cardiovascular
SINGLE SITE FLEXIBLE BLADELESS OBTURATOR
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
SEASPINE MONOPOLAR PROBE SYSYEM
FDA 510(k)
FDA Class 2
·Ear, Nose, Throat
MECTALIF TRANSFORAMINAL INTERBODY FUSION DEVICE 12X30X8 L°
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code MAX·September 14, 2018
20 G X 1.00 IN. (1.1 MM X 25 MM) BD INSYTE¿ AUTOGUARD¿ BC SHIELDED IV CATHETER
FDA Adverse Event
Malfunction
·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·August 23, 2017
INVICTUS SPINAL FIXATION SYSTEM
FDA Adverse Event
Injury
·ALPHATEC SPINE, INC.·Product code NKB·April 30, 2025
35 CM UNIPOLAR LEAD
FDA Adverse Event
Malfunction
·GREATBATCH MEDICAL·Product code DTB·June 14, 2013
HOMECHOICE AUTOMATED PD SET WITH CASSETTE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·July 27, 2011
CARPENTIER-EDWARDS PHYSIO MITRAL ANNULOPLASTY RING
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code KRH·September 29, 2008