7 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Kiierr 272 Laser, Kiierr 148 Laser
FDA 510(k)
FDA Class 2
·Physical Medicine
GE LOGIQ P5 MODEL H44662LD
FDA 510(k)
FDA Class 2
·Radiology
LEMAITRE TT TORTUOUS TRACKER INTRODUCER CATHETER DELIVERY SYSTEM
FDA 510(k)
FDA Class 2
·Cardiovascular
GMK-SPHERE TIBIAL INSERT FIXED SPHERE FLEX SIZE 2/12 MM L
FDA Adverse Event
Malfunction
·MEDACTA INTERNATIONAL SA·Product code JWH·July 23, 2019
HUDSON OXYGEN SUPPLY TUBING, 7'
FDA Adverse Event
Malfunction
·TELEFLEX MEDICAL·Product code BZO·June 17, 2013
CAPTURE-R READY SCREEN 3
FDA Adverse Event
Malfunction
·IMMUCOR, INC.·Product code KSZ·July 28, 2011
E SERIES DEFIBRILLATOR
FDA Adverse Event
Malfunction
·ZOLL MEDICAL CORPORATION·Product code MKJ·September 25, 2008