Scrip is part of Pharma Intelligence UK Limited

This site is operated by Pharma Intelligence UK Limited, a company registered in England and Wales with company number 13787459 whose registered office is 5 Howick Place, London SW1P 1WG. The Pharma Intelligence group is owned by Caerus Topco S.à r.l. and all copyright resides with the group.

This copy is for your personal, non-commercial use. For high-quality copies or electronic reprints for distribution to colleagues or customers, please call +44 (0) 20 3377 3183

Printed By

UsernamePublicRestriction

Medtronic Eyes Proactive Care With Edema Monitoring, MRI-Safe CRM

This article was originally published in The Gray Sheet

Executive Summary

Medtronic is preparing a premarket approval application for its InSync Sentry cardiac resynchronization therapy device/defibrillator with edema monitoring

You may also be interested in...



Medtronic InSync II Protect

Resynchronization defibrillator (CRT), set to launch in Europe this quarter, is among cardiac rhythm management devices previewed during a Feb. 12 earnings call. InSync Protect "will offer unique programming efficiencies and tailored ICD therapy that leverages new clinical findings to minimize unnecessary shocks," CEO Art Collins claims. Medtronic has four CRT-D devices in the pipeline, beginning with InSync Maximo, scheduled for U.S. release this year (1"The Gray Sheet" Jan. 19, 2004, p. 5). Also set for domestic launch this year are six new ICD models, including the Intrinsic "core ICD," and two pacemaker platforms - EnPulse 2 by summer and EnRhythm by year-end...

US Q1 Consumer Health Earnings Preview: Label This One Historic And Challenging But Promising

US OTC drug and supplement firms’ reports of results for the first three months of 2024 began on April 19 with P&G. JP Morgan analysts say while “some retailers in the US in particular” are reducing consumer health inventories, for the overall sector they expect “a healthier balance of positive volume and lower pricing contribution.”

Keeping Track: Cancer Approvals From Lumisight Imaging To Adjuvant Alecensa

The US FDA’s approval of Lumicell’s optical imaging agent Lumisight makes a dozen novel approvals in 2024 for the Center for Drug Evaluation and Research.

Latest Headlines
See All
UsernamePublicRestriction

Register

MT019835

Ask The Analyst

Ask the Analyst is free for subscribers.  Submit your question and one of our analysts will be in touch.

Thank you for submitting your question. We will respond to you within 2 business days. my@email.address.

All fields are required.

Please make sure all fields are completed.

Please make sure you have filled out all fields

Please make sure you have filled out all fields

Please enter a valid e-mail address

Please enter a valid Phone Number

Ask your question to our analysts

Cancel