18 results · 29ms · Sources: EU EUDAMED, 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