Industry Updates

Covidien has launched the Capnostream 20p bedside monitor.

Philips will sell Infraredx’s TVC Imaging System alongside its Allura interventional X-ray systems in North America and Europe.

FDA approves GE Healthcare’s radioactive diagnostic agent GE Healthcare has announced the U.S. Food and Drug Administration (FDA) approval of Vizamyl (Flutemetamol F18 injection), a radioactive diagnostic agent indicated for Positron Emission Tomography (PET) imaging of the brain to estimate beta amyloid neuritic plaque density in adult patients with cognitive impairment who are being evaluated […]

This year’s MD Expo Nashville was a hit from the start.

Under the agreement, Quest will resell Sony diagnostic monitors to qualified channel partners and end-users in the United States.

The U.S. Department of Commerce’s U.S. Commercial Service is helping companies capitalize on market opportunities in Turkey.

MEDIX-LAB, accredited by the CEA/LNE-LNHB, provides access to expert calibrations.

The new “stacked sensor” design of the R/F and MAM sensors prevents the heel effects on the measurements.

FDA says the UDI system has the potential to improve the quality of information in medical device adverse event reports.

An improved software package is available for the ESU-2400 Electrosurgical Unit Analyzer.

Covidien has launched the Capnostream 20p bedside monitor.

Philips will sell Infraredx’s TVC Imaging System alongside its Allura interventional X-ray systems in North America and Europe.

FDA approves GE Healthcare’s radioactive diagnostic agent GE Healthcare has announced the U.S. Food and Drug Administration (FDA) approval of Vizamyl (Flutemetamol F18 injection), a radioactive diagnostic agent indicated for Positron Emission Tomography (PET) imaging of the brain to estimate beta amyloid neuritic plaque density in adult patients with cognitive impairment who are being evaluated […]

This year’s MD Expo Nashville was a hit from the start.

Under the agreement, Quest will resell Sony diagnostic monitors to qualified channel partners and end-users in the United States.

The U.S. Department of Commerce’s U.S. Commercial Service is helping companies capitalize on market opportunities in Turkey.

MEDIX-LAB, accredited by the CEA/LNE-LNHB, provides access to expert calibrations.

The new “stacked sensor” design of the R/F and MAM sensors prevents the heel effects on the measurements.

FDA says the UDI system has the potential to improve the quality of information in medical device adverse event reports.

An improved software package is available for the ESU-2400 Electrosurgical Unit Analyzer.