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Colorful Seal Assurance Supports EU MDR for Device Packaging

Colorful Seal Assurance Supports EU MDR for Device Packaging
healthcarepackaging.com - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from healthcarepackaging.com Daily Mail and Mail on Sunday newspapers.

European medical device regulationsGreen chameleonஐரோப்பிய மருத்துவ சாதனம் ஒழுங்குமுறைகள்பச்சை பச்சோந்தி

Sedgwick s brand protection experts publish the highly anticipated European recall index report

Sedgwick s brand protection experts publish the highly anticipated European recall index report MEMPHIS, Tenn., March 4, 2021 /PRNewswire/ Sedgwick, a leading global provider of technology-enabled risk, benefits and integrated business solutions published their European state of the nation recall index report, explaining the principal cross-industry market trends of 2020 and revealing predictions for 2021. This industry leading research and analysis were designed and delivered by Sedgwick s experts in best practice recall, remediation and retention solutions. Sedgwick works in partnership with clients across all industries to manage the risks and minimize the impacts of in-market business and product crises. Highlights include a look back at 2020 and predictions for 2021:

Kostenloser wertpapierhandelPrnewswire sedgwickMike malaureStone point capitalCarlyle groupEuropean medical device regulationsஸ்டோந் பாயஂட் மூலதனம்கார்லைல் குழுஐரோப்பிய மருத்துவ சாதனம் ஒழுங்குமுறைகள்

Micro Interventional Devices, Inc ™ Announces Submission of CE Mark Technical Documentation for the MIA-T™ Percutaneous Tricuspid Annuloplasty System

Share this article NEWTOWN, Pa., Jan. 28, 2021 /PRNewswire/ Micro Interventional Devices, Inc.™ (MID) announced today that it has submitted the required technical documentation for CE Mark approval for its MIA-T™ Percutaneous Tricuspid Annuloplasty System for tricuspid valve repair to its Notified Body. The receipt of a CE Mark would allow MID to commercialize MIA-T in the European Union in countries governed by the European Medical Device Regulations (MDR). MID is anticipating an approval in 2021. This will enable a treatment option for millions of patients currently at too high a risk to be treated with the standard of care, open surgical repair with cardiopulmonary bypass.

United statesKatherine whitmanMichael whitmanWillard hennemannEuropean unionCompany contactInterventional devices incInterventional devicesPercutaneous tricuspid annuloplasty systemEuropean medical device regulationsTranscatheter tricuspid annular repairDevice regulationMicro interventional devicesTranscatheter cardiac repairஒன்றுபட்டது மாநிலங்களில்க்யாதரிந் விட்மேன்