Food and Drug Administration, Health Commission issued a letter | stop this type of medical equipment

According to the Voice of China, "National News Network," reported in July this year, China Voice had exclusive coverage, '' biological resonance wave detection allergen was not reliable 'message recently, the National Food and Drug General Administration of Supervision and the State Health Commission issued a letter on the Mo La, Baikang and other two therapeutic apparatus is no longer be registered, and stop the equipment beyond the scope of use.

Since 2003, a test called 'biological resonance wave' has been introduced into the country from Germany. Allergy therapy has been introduced in many countries across the country hospital Even the top three hospitals have purchased such devices, which are known as 'biomemory codes' of information once a substance has been in contact with the human body for a number of times, a 'fuze' of allergies that is detected by detecting resonance waves Can find out if it is allergic

Beijing Dermatology Hospital, a doctor said that since the equipment in the hospital, we must believe that 'since a lot of hospitals are in use, the accuracy of the country to your check, you do not have to consider the high accuracy of the instrument, It's a little too sensitive. '

The technology has been introduced, the relevant experts in the field questioned the voice has never stopped.People engaged in long-term Allergen detection work in the national "thousands of people plan" expert Li Jiyang said: 'The human body by some resonance wave interference, which There is no such thing as a medical teaching book, a journal of academic value, and an article of academic value that allergens are caused by material resonance.

Concerned about the CCTV coverage, SFDA said in September this year, such equipment has never been approved for allergen testing and other purposes, and the product registration certificate has expired, such a new biological resonance wave therapy device Of the registration application, Food and Drug Administration will not be approved.

Recently, the State Health Planning Commission formally sent a letter to all local health planning commissions requesting related medical institutions to immediately handle the related disposal of such products. For those products whose registration certificates expire, they should be stopped immediately.