240 results · 31ms · Sources: EU EUDAMED, US FDA

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Mizuho Osi

FDA UDI
TIDI PRODUCTS, LLC·00618125175314·Mizuho Osi Urology Drain Bags Vinyl Sterile Fit...

MIZUHO OSI

FDA UDI
MAYTEX CORPORATION·D806OSI581212·OSI Seat Drape

MIZUHO OSI

FDA UDI
MAYTEX CORPORATION·D806OSI94112·OSI Andrews Frame Seat Drape

MIZUHO OSI

FDA UDI
MAYTEX CORPORATION·D806OSI5817122·OSI Shearguard

MIZUHO OSI

FDA UDI
MAYTEX CORPORATION·D806OSI5324132·OSI Wilson Base Cover

MIZUHO OSI

FDA UDI
MAYTEX CORPORATION·D806OSI5844112·OSI Pad cover

Mizuho Osi

FDA UDI
TIDI PRODUCTS, LLC·01618125175313·Mizuho Osi Urology Drain Bags Vinyl Sterile Fit...

MIZUHO OSI

FDA UDI
MAYTEX CORPORATION·D806OSI5844122·OSI Shearguard

Mizuho OSI®

FDA UDI
Microtek Medical LLC·00748426141395·Patient Isolation Drape, 96 in x 130 in (244 cm...

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