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FDA to carry out joint AAO monitoring instrument plan cataract surgery

The FDA recently released a cataract surgery for monitoring the medical equipment in the plan, aims to early detection to curb toxic eyes room syndrome (TASS) morbidity.


Active TASS plan (PTP) is the first batch of such devices one of the monitoring plan, the FDA, the national centers for disease control and prevention (CDC), the American academy of ophthalmology society (AAO) parties cooperate together. "As baby boomers into an aging population, cataract surgery will increase the number.China digital thermometer This plan to collect information to help the national TASS outbreak of early research and determine whether some medical equipment for the source." FDA equipment and radiation health center China clinical thermometer (CDRH) equipment evaluation place, nerves, eye, ear,China ear thermometer nose and throat equipment director dr Malvina Eydelman press in the FDA warned.


In the past 11 years, TASS explodes into many American patients of anxiety, each year more than 3 million people to cataract surgery, complications often after 48 hours to happen.China digital blood pressure monitor Medscape medical news report said before, the causes and all kinds of pollutants TASS related, these substances often derived from surgical instruments or auxiliary equipment, leading to a number of devices are being recalled. In an effort to solve the problem, CDRH researchers study to determine the cause inflammation some pollutants levelChina digital thermometer manufacturer , and research and development is applicable to manufacturers of new China clinical thermometer manufacturer device testing method to improve the safety.


According to information, inhibits PTP composition aims to improve FDA, CDC and AAO coordination between and communication, including: FDA and AAO cooperation is registered and aims to collect cataract surgery of the applications of the instrument and the patient outcome information; An agreement with the CDC, acquisition and transportation suspicious TASS outbreak specimens to the FDA laboratory for analysis; Testing instrument TASS related pollutants in eye use levels of the standard method.

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