216 results
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42ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
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MODULAR TABLE ADVANCED CONTROL "I" BASE, 120V
FDA Adverse Event
Malfunction
·MIZUHO ORTHOPEDIC SYSTEMS, INC.·Product code JEA·May 25, 2018
TRIOS CERVICAL MANAGEMENT BASE UNIT
FDA Adverse Event
Injury
·MIZUHO ORTHOPEDIC SYSTEMS, INC.·Product code JEA·March 31, 2026
HANA TABLE
FDA Adverse Event
Malfunction
·MIZUHO ORTHOPEDIC SYSTEMS, INC.·Product code FQO·August 26, 2019
TRIOS/STS CHEST PAD SUPPORT PLATE
FDA Adverse Event
Malfunction
·MIZUHO ORTHOPEDIC SYSTEMS, INC.·Product code JEA·February 19, 2020
COUPLER II, MAIN ASSEMBLY
FDA Adverse Event
Malfunction
·MIZUHO ORTHOPEDIC SYSTEMS, INC.·Product code JEA·February 13, 2018
MODULAR TABLE SYSTEM CHEST PLATE
FDA Adverse Event
Malfunction
·MIZUHO ORTHOPEDIC SYSTEMS, INC.·Product code JEA·June 9, 2017
PROBE, DOPPLER
FDA Adverse Event
MIZUHO ORTHOPEDIC SYSTEMS, INC.·Product code JAF·May 10, 2016
ADVANCED CONTROL I-BASE, DC
FDA Adverse Event
Malfunction
·MIZUHO OSI·Product code JEA·December 2, 2022
HANA
FDA Adverse Event
Malfunction
·MIZUHO ORTHOPEDIC SYSTEMS, INC.·Product code JEB·October 16, 2015
MODULAR TABLE ADVANCED CONTROL "I" BASE
FDA Adverse Event
Malfunction
·MIZUHO ORTHOPEDIC SYSTEMS, INC.·Product code JEA·February 7, 2018
ADVANCED CONTROL I-BASE, DC
FDA Adverse Event
Malfunction
·MIZUHO ORTHOPEDIC SYSTEMS, INC.·Product code JEA·August 6, 2024
MIZUHO OSI
FDA Adverse Event
Injury
·Product code JEA·August 5, 2014
MIZUHO OSI
FDA Adverse Event
Malfunction
·MIZUHO OSI·Product code FQO·September 30, 2009
OSI MIZUHO
FDA Adverse Event
Malfunction
·ORTHOPEDIC SYSTEMS INC.·Product code FQO·July 31, 2008
MIZUHO OSI
FDA Adverse Event
Malfunction
·MIZUHO OSI·Product code JEA·June 30, 2016
MIZUHO OSI
FDA Adverse Event
Malfunction
·MIZUHO OSI·Product code JEA·May 25, 2016
MIZUHO OSI
FDA Adverse Event
Injury
·MIZUHO ORTHOPEDIC SYSTEMS, INC.·Product code JEA·May 25, 2018
TRIOS ORTHOPEDIC TRAUMA TOP
FDA Adverse Event
Malfunction
·MIZUHO ORTHOPEDIC SYSTEMS, INC.·Product code JEA·January 20, 2020
HANA SURGICAL TABLE
FDA Adverse Event
Malfunction
·MIZUHO ORTHOPEDIC SYSTEMS, INC.·Product code JEA·June 27, 2018
CLAMP
FDA Adverse Event
Injury
·MIZUHO ORTHOPEDIC SYSTEMS, INC.·Product code JEA·July 19, 2018