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JEM Phase 1

JEM: The world safest subcutaneous, enclosed, biocompatible implantable device, attached directly to a AV fistula or graft or vein, for chronic disease patients in need of repetitive vascular access

Total Cost €

0

EC-Contrib. €

0

Partnership

0

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 JEM Phase 1 project word cloud

Explore the words cloud of the JEM Phase 1 project. It provides you a very rough idea of what is the project "JEM Phase 1" about.

eliminates    vein    blood    back    device    markets       transfusions    standard    longevity    healthcare    pediatric    subcutaneous    technique    made    replacement    200m    digestive    mortality    morbidity    causing    gauge    life    patients    advantages    operations    lowering    blunt    chemotherapy    sold    conservative    potentially    enclosed    home    medical    thereby    prevents    multiplied    8k    implantable    continually    improves    first    times    period    hematomas    provides    graft    offers    attached    market    repair    flow    hemolysis    reduces    disorders    estimate    jem    save    lifespan    dialysis    seek    safer    fistula    victims    oncology    patient    pain    larger    techniques    receiving    easier    solutions    repetitive    risk    medications    usually    universal    needle    requiring    company    spot    reducing    hemodialysis    savings    trained    gold    vascular    puncturing    wall    buttonhole    patented    perforation    designed    accurate    regular    player    position    burn    clinicians    clinical    undergo    specially   

Project "JEM Phase 1" data sheet

The following table provides information about the project.

Coordinator
ACCESS FOR LIFE 

Organization address
address: 11 HAGRA STREET
city: NETANYA
postcode: 4252008
website: n.a.

contact info
title: n.a.
name: n.a.
surname: n.a.
function: n.a.
email: n.a.
telephone: n.a.
fax: n.a.

 Coordinator Country Israel [IL]
 Project website http://www.accessforlife.biz/testimonials
 Total cost 71˙429 €
 EC max contribution 50˙000 € (70%)
 Programme 1. H2020-EU.2.1.4. (INDUSTRIAL LEADERSHIP - Leadership in enabling and industrial technologies – Biotechnology)
2. H2020-EU.2.3.1. (Mainstreaming SME support, especially through a dedicated instrument)
 Code Call H2020-SMEINST-1-2016-2017
 Funding Scheme SME-1
 Starting year 2016
 Duration (year-month-day) from 2016-06-01   to  2016-11-30

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    ACCESS FOR LIFE IL (NETANYA) coordinator 50˙000.00

Map

 Project objective

'JThe JEM project aims to bring to the healthcare and medical device markets the first subcutaneous enclosed implantable device attached directly to a vein, fistula or graft. The JEM is based on a patented design that greatly improves repetitive vascular access techniques and provides safer, more accurate and effective results. The JEM provides the following advantages: • It is based on the European Gold Standard 'buttonhole technique' for vascular access. • It greatly reduces costs by reducing the need for fistula repair & replacement. • It enables repetitive puncturing at the same spot by less-trained clinicians. • Its 6-year lifespan, 3 times the average fistula lifespan, reduces mortality & morbidity. • Its specially designed needle prevents back wall perforation and hematomas. • It will allow for a larger gauge needle thereby potentially increasing blood flow and lowering the risk of hemolysis. • It can be made to use a unique blunt needle that is sold by Access for Life, causing less pain to the patients ensuring easier and safer home hemodialysis. JEM devices from Access for Life are designed for all patients in need of repetitive vascular access: hemodialysis patients, oncology patients receiving chemotherapy, patients with blood disorders, patients requiring regular medications or blood transfusions, burn victims, pediatric patients and patients with digestive disorders. Due to its longevity, JEM eliminates three of the four operations dialysis patients usually undergo in a 6-year period. This will save healthcare systems about 5,8K € per dialysis patient. Multiplied by the growing number of patients, a conservative estimate of potential savings is over 200M € a year. Through the JEM project, we seek to position our company as the leading player in medical devices for repetitive vascular access, a market that is continually growing. Access for Life offers universal solutions for a wide range of clinical applications that require vascular access.'

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The information about "JEM PHASE 1" are provided by the European Opendata Portal: CORDIS opendata.

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