113 results
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20ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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MDF REVISION HIP SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587P0811240·8mm PLIF Implant 11mm Wide 24mm Length
TASMIN R 8°
FDA UDI
SIGNUS Medizintechnik GmbH·04047844014721·The basic shape of the TASMIN R devices is a ho...
SchureMed
FDA UDI
SCHUERCH CORPORATION·00810014609720·MAQUET 3" SOFTCARE
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587P08112470·8mm PLIF Implant 11mm Wide 24mm Length 7 Degrees
FIX-L PEEK PLIF and T-PLIF System
FDA UDI
Jeil Medical Corporation·08800089473175·
FIX-L PEEK PLIF and T-PLIF System
FDA UDI
Jeil Medical Corporation·08800089473182·
FIX-L PEEK PLIF and T-PLIF System
FDA UDI
Jeil Medical Corporation·08800089473199·
FIX-L PEEK PLIF and T-PLIF System
FDA UDI
Jeil Medical Corporation·08800089473168·
FIX-L PEEK PLIF and T-PLIF System
FDA UDI
Jeil Medical Corporation·08800089473205·
FIX-L PEEK PLIF and T-PLIF System
FDA UDI
Jeil Medical Corporation·08800089473229·
FIX-L PEEK PLIF and T-PLIF System
FDA UDI
Jeil Medical Corporation·08800089473236·
FIX-L PEEK PLIF and T-PLIF System
FDA UDI
Jeil Medical Corporation·08800089473212·
FIX-L PEEK PLIF and T-PLIF System
FDA UDI
Jeil Medical Corporation·08800089473243·
POLARIS 95000-A BEDSIDE/TRANSPORT MONITOR
FDA 510(k)
FDA Class 2
·Cardiovascular
ACCUFIX TILTING RADIOTRANSLUCENT HEADHOLDER
FDA 510(k)
FDA Class 2
·Radiology
ENDOTRACH TUBE 8229507 CONTACT EMG 7MM
FDA Adverse Event
Injury
·MEDTRONIC XOMED, INC.·Product code ETN·January 7, 2014
NIM® 3.0 INTERFACE
FDA Adverse Event
Malfunction
·MEDTRONIC XOMED INC.·Product code ETN·November 29, 2017
NIM® 3.0 MAINFRAME
FDA Adverse Event
Malfunction
·MEDTRONIC XOMED INC.·Product code ETN·June 16, 2017
NIM® 3.0 MAINFRAME
FDA Adverse Event
Malfunction
·MEDTRONIC XOMED INC.·Product code ETN·December 8, 2017