10,000 results · 28ms · Sources: EU EUDAMED, US FDA

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Neurolyser XR DQA

Device
EU MDR · Eu Md Class 1 ·FUSMOBILE ISRAEL LTD·On the market·1 country

NEURO DQA PHANTOM GEL

FDA UDI
INSIGHTEC LTD·07290015461207·DQA phantom (tissue mimic) gel for calibration ...

Neurolyser XR DQA Assembly

FDA UDI
FUSMobile LTD·07290019747031·

Exablate DQA Phantom Gel

FDA UDI
INSIGHTEC LTD·07290015461214·Tissue mimic phantom gel for DQA for Body appli...

DQA PHANTOM

FDA Adverse Event
Injury ·GE HEALTHCARE TECHNOLOGIES·Product code LNH·February 24, 2005

LIFECODES HLA-DQA1/B1 SSO TYPING KIT

FDA Adverse Event
Malfunction ·IMMUCOR GTI DIAGNOSTICS, INC.·Product code MZI·May 24, 2018

LIFECODES HLA-DQA1/B1 SSO TYPING KIT

FDA Adverse Event
Malfunction ·IMMUCOR GTI DIAGNOSTICS, INC.·Product code MZI·September 14, 2018

HIART SYSTEM

FDA Adverse Event
Malfunction ·TOMOTHERAPY INCORPORATED·Product code IYE·December 8, 2009

LIFECODES HLA DQAB

FDA Adverse Event
Malfunction ·IMMUCOR GTI DIAGNOSTICS, INC.·Product code MZI·February 27, 2019

IMMULITE 2500 STAT TROPONIN I

FDA Adverse Event
Other ·SIMENS HEALTHCARE DIAGNOSTICS INC.·Product code JHX·March 24, 2010

RD SET YI

FDA Adverse Event
Malfunction ·MASIMO - 52 DISCOVERY·Product code DQA·March 29, 2021

MR TWINSPEED

FDA Adverse Event
Malfunction ·GE MEDICAL SYSTEMS, LLC·Product code LNH·May 7, 2012

KELLER FUNNEL2 (1PK)

FDA Adverse Event
Malfunction ·ALLERGAN (KELLER)·Product code KDD·January 4, 2024

RD SET TC-I

FDA Adverse Event
Malfunction ·MASIMO - 40 PARKER·Product code DPZ·February 21, 2018

KELLER FUNNEL2 (5PK)

FDA Adverse Event
Malfunction ·ALLERGAN (KELLER)·Product code KDD·February 27, 2024

SEDLINE SENSOR

FDA Adverse Event
Malfunction ·MASIMO - 40 PARKER·Product code MWI·January 31, 2018

RESOLUTION CLIP

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code PKL·December 10, 2024

VERSASTEP 5MM SGLUSE SHORT DIL/CANN EXPSL

FDA Adverse Event
Malfunction ·COVIDIEN·Product code GCJ·March 16, 2015

Neurolyser XR DQA

Basic UDI-DI
EU MDR · Eu Md Class 1 ·FUSMOBILE ISRAEL LTD·1 device

EXABLATE 2000

FDA Adverse Event
Malfunction ·INSIGHTEC, LTD.·Product code NRZ·May 31, 2011