115 results · 54ms · Sources: EU EUDAMED, US FDA

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OHIO MEDICAL PRODUCTS

FDA Adverse Event
Injury ·OHIO MEDICAL PRODUCTS·Product code BTI·February 28, 2013

AMVEX FLOWMETER

FDA Adverse Event
Death ·OHIO MEDICAL LLC·Product code CAX·February 21, 2021

OHIO MEDICAL

FDA Adverse Event
Malfunction ·Product code KFZ·May 20, 2021

OHIO MEDICAL TWIN FLOWMETER

FDA Adverse Event
Malfunction ·OHIO MEDICAL LLC·Product code CAX·February 9, 2022

OHMEDA

FDA Adverse Event
Malfunction ·OHIO MEDICAL CORPORATION·Product code CAX·November 9, 2011

DISS VACUUM LATCH VALVE

FDA Adverse Event
Other ·OHIO MEDICAL CORPORATION·Product code BTA·December 13, 2010

OHMEDA 1251 CONTINUOUS/INTERMITTENT VACUUM REGULATOR

FDA Adverse Event
Malfunction ·OHIO MEDICAL PRODUCTS·Product code KDP·October 21, 2019

7800 VENTILATOR

FDA Adverse Event
Malfunction ·OHIO MEDICAL PRODUCTS·Product code CBK·February 4, 1993

INTERMITTENT SUCTION REGULATOR

FDA Adverse Event
Malfunction ·OHIO MEDICAL CORPORATION·Product code KDP·May 7, 2007

OHIO MEDICAL

FDA Adverse Event
Other ·OHIO MEDICAL CORPORATION·Product code KDP·June 1, 2009

AMVEX OXYGEN FLOWMETER

FDA Adverse Event
Death ·OHIO MEDICAL LLC·Product code CAX·February 9, 2018

SMART PORT CT

FDA Adverse Event
Injury ·ANGIODYNAMICS, INC.·Product code LJT·May 20, 2026

AMVEX

FDA Adverse Event
Malfunction ·OHIO MEDICAL LLC·Product code CAX·April 23, 2025

MEDICAL GAS FLOWMETER

FDA Adverse Event
Injury ·OHIO MEDICAL LLC·Product code CAX·August 24, 2023

PUMP, INFUSION, IMPLANTED, PROGRAMMABLE

FDA Adverse Event
Malfunction ·MEDTRONIC NEUROMODULATION·Product code LKK·March 9, 2015

MEDEX CLEAR CUFF PRESSURE INFUSION

FDA Adverse Event
Malfunction ·SMITHS MEDICAL ASD, INC.·Product code KZD·December 26, 2024

OHIO TRANSPORT INCUBATOR

FDA Adverse Event
Malfunction ·OHIO MEDICAL PRODUCT OHMEDA CO.·Product code FPL·June 26, 1998

MEDEX C FUSOR 500ML PRESSURE INFUSOR

FDA Adverse Event
Malfunction ·SMITHS MEDICAL ASD, INC.·Product code KZD·November 20, 2024

OHIO MEDICAL COLLECTION BOTTLE

FDA Adverse Event
Malfunction ·OHIO MEDICAL LLC·Product code KDQ·September 14, 2017

OMI 7300 OPERATING TABLE

FDA Adverse Event
Other ·OHIO MEDICAL INSTRUMENT CO., INC.·Product code GDC·April 21, 2003