Airgas creates new healthcare focused brand

Airgas has created a new brand called Airgas Healthcare that will integrate existing healthcare and life sciences activity of Airgas and Air Liquide Healthcare. Airgas Healthcare will provide a wide range of medical gasses and related products and services to customers with the integration of Air Liquide Healthcare. Those who will benefit from the new

Study shows benefits of overhead utility systems in ICUs

A new study from Draeger and Georgia Tech has shown that overhead utility systems potentially have substantial benefits in intensive care unit rooms. The study claims that ceiling mounted solutions for utilities are more superior than a traditional headwall. Hospital staff members tend to like overhead booms more, according to the study. Overhead booms have shown

Steute Meditech: How navigation aids ease foot switch usability

The ever-increasing functional capabilities of emerging medical devices have precipitated new requirements for the multi-function foot controls used to operate the equipment. These foot controls typically consist of multiple actuators … one for each required control function. For example, it is not uncommon to find foot controls for electrosurgical generators with 3 functions, foot controls

G4S launches new portable security system to protect patients

G4S, an integrated security company, has launched a portable monitoring system for vulnerable patients who have psychiatric disorders or cognitive conditions. Virtual Patient Watch is a security system that monitors patients and sends out an alarm if someone tries to get out of bed or has behavior that requires immediate medical attention. It is designed

Why our grandkids will laugh at today’s surgical robots

For the last 10 years, if anyone mentioned robotic surgery or surgical robots, 95% of the time they meant the da Vinci robot from Intuitive Surgical. “That product has been so dominantly successful that almost everybody who talks about it is talking with that as their reference point,” said Roger Smith, chief technology officer for

How medtech companies can benefit from agile marketing

Getting a medical device to market can be tough. It has to go through several hoops at the FDA, including the 5-step premarket requirements that include: classifying the device; choosing the correct premarket submission; preparing appropriate information for premarket FDA submission; sending a premarket submission to the FDA and communicating with FDA staff during review; and

Medtech stories we missed this week: April 21, 2017

From new and renewed partnerships to FDA approvals, here are medtech stories we missed this week but thought were still worth mentioning. 1. Life Spine receives FDA clearance for cervical spacer system Life Spine announced in an April 19 press release that it has received FDA 510(k) clearance for its Plateau-C Ti Cervical Spacer System. The system uses

Medtech stories we missed this week: April 14, 2017

From FDA approvals to business expansion plans, here are medtech stories we missed this week but thought were still worth mentioning. 1. BioTelemetry launches offer to acquire LifeWatch BioTelemetry and LifeWatch announced in an April 9 press release that the 2 companies have entered a transaction agreement that states BioTelemetry will launch a tender offer to acquire all

Trinseo offers medical grade MAGNUM ABS for medical equipment

Trinseo, a global materials company and manufacturer of plastics, latex binders and synthetic rubber, is offering medical equipment manufacturers and molders medical-grade MAGNUM ABS Resins. The material features the advantages of Trinseo’s mass polymerization technology combined with the properties needed most for medical applications to assure the integrity of end-use applications. Trinseo’s MAGNUM 8391 MED ABS Resins

RJG now offers Mold Design course

RJG, Inc. held their first Mold Design class in March of this year. The goal of offering this course is to provide mold makers, design engineers and molders with the common language and core knowledge required to design injection molds that exceed time, cost and quality requirements. Mold Design is meant to bridge the gap

Fluid Metering has new valveless waste transfer pump

Fluid Metering is touting a new valveless waste transfer pump that is designed to remove waste fluid created by medical diagnostic instrumentation while analyzing patient fluid samples. Waste fluid usually has a mixture of patient samples, like blood components and urine samples, that get combined with reagents, byproducts of reagent reactions and wash fluids. The

Masimo touts adult EEG sensor

Masimo has announced that its RD SedLine EEG sensor is now available in the U.S. The EEG sensor is meant to be used with Masimo SedLine Brain Function Monitoring and is compatible with the O3 Regional Oximetry offered by Masimo. The SedLine and O3 monitor onto the Masimo Root monitoring platform to help clinicians obtain

Fibrosis: How to prevent it in medical device implants

Massachusetts Institute of Technology (MIT) and Boston Children’s Hospital researchers have discovered a way to prevent fibrosis from forming around medical device implants. The body’s immune system usually attacks implanted medical devices that are used for drug delivery, sensing or tissue regeneration. Defense cells in the body try to isolate the foreign material from devices

MedLumics secures 34.4M Euros in Series B funding

MedLumics, a cardiac device company specializing in optically guided minimally invasive instruments, announced that it has raised 34.4M Euros in financing that will be used to help advance the product and clinical development of the company’s AblaView catheter, intended for the treatment of atrial fibrillation (AF) and other arrhythmias. This financing is the largest in

Medtech stores we missed this week: March 10, 2017

The FDA and Health Canada cleared a couple medical devices while other companies touted their device studies. Here are medtech stories we missed this week but were still worth mentioning. 1. FDA clears Medela’s neonatal enteral feeding device Medela has received 510(k) clearance from the FDA to market its ENFit Low Dose Tip eternal syringes,