54 results · 55ms · Sources: EU EUDAMED, US FDA

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SENSONICS, INTERNATIONAL

FDA registration
SENSONICS, INTERNATIONAL·4 products·🇺🇸 United States

EVERSENSE SENSOR

FDA Adverse Event
Malfunction ·SENSEONICS INC.·Product code SBA·February 6, 2025

EVERSENSE SENSOR

FDA Adverse Event
Malfunction ·SENSEONICS INC.·Product code SBA·February 4, 2025

EVERSENSE SENSOR

FDA Adverse Event
Malfunction ·SENSEONICS INC.·Product code QHJ·February 4, 2025

EVERSENSE SENSOR

FDA Adverse Event
Malfunction ·SENSEONICS INC.·Product code SBA·February 12, 2025

EVERSENSE SENSOR

FDA Adverse Event
Malfunction ·SENSEONICS INC.·Product code SBA·April 28, 2025

MedEnvoy Global BV

Authorized representative
🇳🇱 Netherlands·143 Manufacturers·2306 Devices

SleepScout

FDA UDI
Cleveland Medical Devices Inc.·B14360201292·Optional accessory kit for use with SleepScout ...

Emergo Europe B.V.

Authorized representative
🇳🇱 Netherlands·900 Manufacturers·22100 Devices

OPTIFLUX 180NRE DIALYZER FINISHED ASSY.

FDA Adverse Event
Malfunction ·OGDEN MANUFACTURING PLANT·Product code KDI·August 22, 2024

G2 X FILTER SYSTEM - FEMORAL

FDA Adverse Event
Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code DTK·August 2, 2021

G2 EXPRESS FILTER SYSTEM - FEMORAL

FDA Adverse Event
Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code DTK·March 11, 2022

X-STOP IPD SYSTEM

FDA Adverse Event
Injury ·MEDTRONIC SPINE LLC·Product code NQO·December 31, 2009

MICRO-INTRODUCER

FDA Adverse Event
Injury ·VASCULAR SOLUTIONS, INC.·Product code DYB·July 10, 2018

MedEnvoy Global BV

Importer
🇳🇱 Netherlands·234 Manufacturers

G2 EXPRESS FILTER SYSTEM - FEMORAL

FDA Adverse Event
Injury ·BARD PERIPHERAL VASCULAR, INC.·Product code DTK·October 13, 2020

G2 EXPRESS FILTER SYSTEM - FEMORAL

FDA Adverse Event
Injury ·BARD PERIPHERAL VASCULAR, INC.·Product code DTK·January 13, 2021

G2 FILTER SYSTEM - JUGULAR

FDA Adverse Event
Death ·BARD PERIPHERAL VASCULAR, INC.·Product code DTK·July 1, 2019

DIALYSIS UNKNOWN

FDA Adverse Event
Death ·COVIDIEN LLC·Product code MSD·June 10, 2025

LIFESTREAM

FDA Adverse Event
Malfunction ·CLEARSTREAM TECHNOLOGIES LTD.·Product code PRL·November 9, 2017