9 results
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27ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Bencox M Stem Lateralized & Bencox Mirabo Cup System
FDA 510(k)
FDA Class 2
·Orthopedic
Avalign
FDA UDI
Avalign Technologies, Inc.·00190776020415·Keyhole Bracket
ONE TOUCH ULTRA
FDA Adverse Event
Malfunction
·LIFESCAN, INC.·Product code CFR·June 14, 2002
MEDIC4ALL TELEMEDICINE SYSTEM, MODEL VMS-01 (NIBP)
FDA 510(k)
FDA Class 2
·Cardiovascular
ENDOTRACHEAL TUBE CHANGERS
FDA 510(k)
FDA Class 2
·Anesthesiology
STAPLE, IMPLANTABLE
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code GDW·October 10, 2014
9600
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS·Product code JAA·June 3, 2013
TRANSITION 6.5MM HA POLYAXIAL PEDICLE SCREW 45
FDA Adverse Event
Injury
·GLOBUS MEDICAL, INC.·Product code NQP·July 7, 2011
Aquapak 340 SW, 340, mL w/040 Adaptor, Teleflex Medical, respiratory gas humidifier adaptor.
FDA Enforcement
Class II
·Terminated·Teleflex Medical·July 16, 2014