34 results
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24ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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GARMENT ELECTRODES
FDA 510(k)
FDA Class 2
·Neurology
PROWESS PANTHER PROARC, MODEL VERSION 5.0
FDA 510(k)
FDA Class 2
·Radiology
DELTA T
FDA 510(k)
FDA Class 2
·Anesthesiology
Widex
FDA UDI
Widex A/S·05706069886559·WIDEX MOMENT MRB0 (Sporty red ) 440, RIC 10
Widex
FDA UDI
Widex A/S·05706069812565·Widex EVOKE E-PA (Sporty red ) 440, RC coil
CHARGING SYSTEM
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·May 24, 2013
GE OEC 9900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·September 3, 2008
MALLINCKRODT
FDA Adverse Event
Injury
·COVIDIEN, FORMERLY TYCOHEALTHCARE·Product code BTR·June 21, 2011
SUPERSHEATH
FDA Adverse Event
Malfunction
·TOGO MEDIKIT CO. LTD.·Product code DRE·December 2, 2016
SUPER SHEATH
FDA Adverse Event
Injury
·TOGO MEDIKIT CO., LTD.·Product code DRE·June 2, 2022
SUPERSHEATH
FDA Adverse Event
Injury
·TOGO MEDIKIT CO. LTD.·Product code DRE·August 12, 2018
SUPERSHEATH
FDA Adverse Event
Malfunction
·TOGO MEDIKIT CO. LTD.·Product code DRE·December 11, 2016
SUPER SHEATH
FDA Adverse Event
Injury
·TOGO MEDIKIT CO.LTD.·Product code DRE·January 18, 2018
SUPER SHEATH
FDA Adverse Event
Injury
·TOGO MEDIKIT CO., LTD.·Product code DRE·March 21, 2023
SUPER SHEATH
FDA Adverse Event
Injury
·TOGO MEDIKIT CO. LTD.·Product code DRE·April 28, 2020
SUPERSHEATH
FDA Adverse Event
Injury
·TOGO MEDIKIT CO. LTD.·Product code DRE·April 11, 2017
SUPER SHEATH
FDA Adverse Event
Injury
·TOGO MEDIKIT CO. LTD.·Product code DRE·February 11, 2020
SUPER SHEATH
FDA Adverse Event
Injury
·TOGO MEDIKIT CO., LTD.·Product code DRE·January 19, 2023
SUPER SHEATH
FDA Adverse Event
Injury
·TOGO MEDIKIT CO. LTD.·Product code DRE·December 12, 2019
SUPER SHEATH
FDA Adverse Event
Injury
·TOGO MEDIKIT CO., LTD.·Product code DRE·July 19, 2022