10,000 results
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64ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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LightForce FXi
FDA UDI
LITECURE LLC·00854103007042·Infrared phototherapy device emitting up to 15 ...
LightForce FXi
FDA UDI
LITECURE LLC·00854103007097·Infrared phototherapy device emitting up to 15 ...
SPECTRA OPTIA
FDA Adverse Event
Injury
·TERUMO BCT·Product code LKN·June 6, 2024
BD BACTEC FXI Culture System
FDA 510(k)
FDA Class 1
·Microbiology
HISPEED FXI
FDA Adverse Event
Malfunction
·GE YOKOGAWA MEDICAL SYSTEMS, LTD.·Product code JAK·September 19, 2008
PROCAIR PLUS MATTRESS
FDA Adverse Event
Injury
·FXI·Product code FNM·January 20, 2017
DERMAFLOAT LAL SYSTEM
FDA Adverse Event
Malfunction
·FXI·Product code FNM·January 7, 2019
DERMAFLOAT LAL SYSTEM
FDA Adverse Event
Malfunction
·FXI·Product code FNM·August 16, 2018
DERMAFLOAT LAL SYSTEM
FDA Adverse Event
Malfunction
·FXI·Product code FNM·August 29, 2018
AIR MATTRESS AND CONTROL UNIT
FDA Adverse Event
Injury
·FXI·Product code FNM·September 27, 2018
PROCAIR PLUS MATTRESS
FDA Adverse Event
Injury
·FXI·Product code FNM·February 21, 2020
DERMAFLOAT LAL SYSTEM
FDA Adverse Event
Malfunction
·FXI·Product code FNM·March 27, 2020
DERMAFLOAT LAL SYSTEM
FDA Adverse Event
Malfunction
·FXI·Product code FNM·March 9, 2018
STRYKER AIR II SYSTEM
FDA Adverse Event
Malfunction
·FXI·Product code FNM·September 30, 2019
DERMAFLOAT LAL SYSTEM
FDA Adverse Event
Malfunction
·FXI·Product code FNM·September 30, 2019
DERMAFLOAT LAL SYSTEM
FDA Adverse Event
Malfunction
·FXI·Product code FNM·September 30, 2019
DERMAFLOAT LAL SYSTEM
FDA Adverse Event
Injury
·FXI·Product code FNM·July 15, 2019
HISPEED LX//I, HISPEED FX/I, AND HISPEED DX/I FAMILY OF SYSTEMS
FDA 510(k)
FDA Class 2
·Radiology
BD VACUTAINER 9NC 0.5 ML BUFFERED TRISODIUM CITRATE BLOOD COLLECTION TUBE
FDA Adverse Event
Malfunction
·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·August 18, 2021
EVOLUT FX DCS
FDA Adverse Event
Malfunction
·MEDTRONIC HEART VALVES DIVISION·Product code NPT·May 17, 2023