16 results
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18ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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FEP RINGED GORE-TEX VASCULAR GRAFT
FDA 510(k)
FDA Class 2
·Cardiovascular
SOCKET COMBO POST ALIMED 2/CS
FDA UDI
ALIMED, INC.·00733657240627·
ILT CO2 SURGICAL LASER FOR ORAL SOFT TISSUE PROCED
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
LYTENING TM 6/R
FDA 510(k)
FDA Class 2
·Clinical Chemistry
MAINFRAME 8253001 NIM RESPONSE 3.0
FDA Adverse Event
Injury
·MEDTRONIC XOMED, INC·Product code ETN·November 7, 2013
NIM® EMG - ENDOTRACHEAL TUBE - TRIVANTAGE®
FDA Adverse Event
Malfunction
·MEDTRONIC XOMED INC.·Product code ETN·June 3, 2015
MAINFRAME 8253001 NIM RESPONSE 3.0
FDA Adverse Event
Injury
·MEDTRONIC XOMED, INC·Product code ETN·December 16, 2013
8800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·January 4, 2013
CLEAR, PVC CONTRAST INJECTION LINE
FDA Adverse Event
Malfunction
·MERIT MEDICAL SYSTEMS, INC.·Product code DXJ·November 29, 2010
SPECTRUM INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORP·Product code FRN·February 4, 2014
NIM® 3.0 MAINFRAME
FDA Adverse Event
Injury
·MEDTRONIC XOMED INC.·Product code ETN·January 14, 2015
ENDOTRACH TUBE 8229507 CONTACT EMG 7MM
FDA Adverse Event
Injury
·MEDTRONIC XOMED, INC.·Product code ETN·January 7, 2014
NIM® EMG ELECTRODE
FDA Adverse Event
Malfunction
·MEDTRONIC XOMED INC.·Product code GXZ·January 27, 2017
NIM® EMG - ENDOTRACHEAL TUBE - TRIVANTAGE®
FDA Adverse Event
Injury
·MEDTRONIC XOMED, INC·Product code ETN·July 1, 2016
NIM® EMG - ENDOTRACHEAL TUBE - TRIVANTAGE®
FDA Adverse Event
Malfunction
·MEDTRONIC XOMED INC.·Product code ETN·December 8, 2016
NIM® EMG ELECTRODE
FDA Adverse Event
Malfunction
·MEDTRONIC XOMED INC.·Product code GXZ·February 13, 2017