18 results
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29ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ENTREE NEEDLE
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
PANOSOL II UVA-218
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
SDU 500 DIAGNOSTIC ULTRASOUND INSTRUMENT
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
RADIANCE
FDA Adverse Event
Malfunction
·RADIOMETER MEDICAL APS·Product code LNX·July 27, 2006
MAINFRAME 8253001 NIM RESPONSE 3.0
FDA Adverse Event
Injury
·MEDTRONIC XOMED, INC·Product code ETN·November 7, 2013
RADIANCE
FDA Adverse Event
Malfunction
·RADIOMETER MEDICAL APS·Product code LNX·January 31, 2007
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
ACTIVA
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code MHY·January 14, 2013
SUTURE TRIMMER
FDA Adverse Event
Injury
·AV-REDWOOD CITY·Product code MGB·December 3, 2010
BMT SPLINED KNEE STM 12X120
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JWH·July 3, 2014
NIM® 3.0 MAINFRAME
FDA Adverse Event
Injury
·MEDTRONIC XOMED INC.·Product code ETN·January 14, 2015
SROM*STM ST,36+8L NK,18X13X160
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC. 1818910·Product code JDI·January 28, 2019
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