90 results
·
32ms
·
Sources: EU EUDAMED, US FDA
MODIFICATION TO N PROTEIN STANDARD SL
FDA 510(k)
FDA Class 2
·Clinical Chemistry
PedFuse®
FDA UDI
SPINEFRONTIER, INC.·00190361011743·PedFuse Respond, CNL, 8.0mm x 70mm
R & D 4K RETIC
FDA 510(k)
FDA Class 2
·Hematology
M2424A SONOS 5500/4500 DIAGNOSTIC ULTRASOUND SYSTEM, VERSION B.2. 21330A TRANSDUCER
FDA 510(k)
FDA Class 2
·Radiology
LIGASURE
FDA Adverse Event
Malfunction
·COVIDIEN MEDICAL PRODUCTS·Product code GEI·April 17, 2018
LIGASURE
FDA Adverse Event
Malfunction
·COVIDIEN MEDICAL PRODUCTS·Product code GEI·October 7, 2020
LIGASURE
FDA Adverse Event
Injury
·COVIDIEN MEDICAL PRODUCTS·Product code GEI·July 21, 2018
LIGASURE
FDA Adverse Event
Malfunction
·COVIDIEN MEDICAL PRODUCTS·Product code GEI·February 20, 2018
LIGASURE
FDA Adverse Event
Malfunction
·COVIDIEN MEDICAL PRODUCTS·Product code GEI·November 26, 2018
MONOCRYL POLIGLECAPRONE 25 SUTURE UNKNOWN PRODUCT
FDA Adverse Event
Injury
·ETHICON INC.·Product code GAN·August 8, 2018
ETHIBOND EXTRA & EXCEL POLYESTER SUTURE UNKNOWN
FDA Adverse Event
Injury
·ETHICON INC.·Product code GAT·August 8, 2018
LIGASURE
FDA Adverse Event
Malfunction
·COVIDIEN MEDICAL PRODUCTS·Product code GEI·June 9, 2021
LIGASURE
FDA Adverse Event
Malfunction
·COVIDIEN MEDICAL PRODUCTS·Product code GEI·February 2, 2018
LIGASURE
FDA Adverse Event
Malfunction
·COVIDIEN MEDICAL PRODUCTS·Product code GEI·November 13, 2018
LIGASURE
FDA Adverse Event
Malfunction
·COVIDIEN MEDICAL PRODUCTS·Product code GEI·April 16, 2019
INSET 30
FDA Adverse Event
Malfunction
·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·August 11, 2025
LIGASURE
FDA Adverse Event
Malfunction
·COVIDIEN MFG DC BOULDER·Product code GEI·April 24, 2020
LIGASURE
FDA Adverse Event
Malfunction
·COVIDIEN MFG DC BOULDER·Product code GEI·March 14, 2019
LIGASURE
FDA Adverse Event
Malfunction
·COVIDIEN MEDICAL PRODUCTS·Product code GEI·June 16, 2021
CHARGING SYSTEM
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·March 15, 2013