Question 1: What does medical device YZB mean? Medical device products are not standardized or the registration standards compiled by national standard enterprises themselves according to relevant standards, that is, enterprise standards. YZB refers to the registration standards of medical device enterprises.

Question 2: What does medical device business scope 68 mean? Business scope of Medical Device Business License

Class III:

684 ophthalmic surgical devices.

6815 injection puncture instrument

6821 medical electronic instrument

6822 medical optical instrument, Instruments and endoscopic equipment

6823 medical ultrasonic instruments and related equipment

6824 medical laser instruments and equipment

6825 medical high-frequency instruments and equipment

6826 physical therapy and rehabilitation equipment

6828 medical magnetism * * * Vibration equipment

683 medical X-ray equipment

6832 medical high-energy X-ray equipment

6833 medical nuclide equipment

684 clinical laboratory analysis instrument

6845 extracorporeal circulation and blood processing equipment

6846 implant materials and artificial organs

6854 operating room, emergency room, Clinic equipment and appliances

6858 medical cold therapy, cryogenic and refrigeration equipment and appliances

6863 stomatological materials

6864 medical sanitary materials and dressings

6865 medical suture materials and adhesives

6866 medical polymer materials and products

687 software

6877 interventional equipment

Question 3. Where's the picture?

Question 4: What does the quasi-brand name of medical devices mean? 1. The quasi-brand name of national medicine is the drug production approval number obtained by the drug production unit after strict examination and approval by the State Food and Drug Administration before producing new drugs, which is equivalent to a person's ID card. Its format is: Chinese medicine quasi-character +1-digit letter +8-digit number, in which the letter used for chemicals is "H", the letter used for Chinese medicine is "Z" and so on. Only by obtaining this approval number can drugs be produced and sold. Due to historical reasons, provincial drug authorities used to have the right to approve drugs, and some drugs used local approval numbers, such as "Jingwei Drug Zhunzi" and "Huwei Drug Zhunzi". These drugs are approved according to the local drug standards of provinces and municipalities directly under the Central Government, which is not conducive to the unified management of drugs by the state. In order to ensure the safety of clinical medication, after 1999, the state upgraded the past local drug standards to national drug standards, cleaned up and rectified the drugs in the format of "X (provincial) standard for defending drugs", issued the approval number of "National Medicine Standard" for drugs that met the national standards, and eliminated drugs that did not meet the national standards. At the same time, the authority for approving new drugs was assigned to the State Food and Drug Administration. According to the current Drug Administration Law, the production of drugs "needs to be approved by the drug supervision and administration department of the State Council, and a drug approval number will be issued". Therefore, if we find drugs with the approval number of "X Wei Yao Zhunzi" and other non-"National Medicine Zhunzi" in the market now, they can all be regarded as counterfeit drugs because the expiry date stipulated by National Medical Products Administration has passed. When people buy medicine, they must carefully watch the approval number. Don't buy drugs without approval number or with questionable approval number, so as not to buy fake drugs. Code of standard Chinese medicine: the format of drug approval number is "standard Chinese medicine (test) word+letter+8 digits". Among them, "medicine" stands for medicine, which is the most basic property (different from health food and medical devices), "quasi" stands for drugs approved for production by the state, and "trial" stands for drugs approved for trial production by the state. The letters include H, Z, S, B, T, F and J, which respectively represent different categories of drugs: H stands for chemicals, Z stands for Chinese patent medicines, S stands for biological products, B stands for health care drugs, T stands for in vitro chemical diagnostic reagents, F stands for pharmaceutical excipients, and J stands for imported repackaged drugs. The first and second digits of the 8 digits represent the source of the original approval number, and 1 of them represent the drugs approved by the former Ministry of Health; 19, 2 on behalf of the national drug regulatory authorities approved drugs; 11 Beijing, 12 Tianjin, 13 Hebei, 14 Shanxi, 15 Inner Mongolia, 21 Liaoning, 22 Jilin, 23 Heilongjiang, 31 Shanghai, 32 Jiangsu, 33 Zhejiang, 34 Anhui, 35 Fujian, 36 Jiangxi, 37 Shandong, 41 Henan, 42 Hubei, 43 Hunan, 44 Hubei. 46 Hainan Province, 5 Chongqing City, 51 Sichuan Province, 52 Guizhou Province, 53 Yunnan Province, 54 *** Autonomous Region, 61 Shaanxi Province, 62 Gansu Province, 63 Qinghai Province, 64 Ningxia * * * Autonomous Region, 65 Xinjiang * * * Er Autonomous Region. The 3rd and 4th delegates renewed the last two digits of the year of the approval number, but the approval number from the Ministry of Health and the State Drug Administration still used the last two digits of the original number. The 5th, 6th, 7th and 8th digits are the serial numbers of the approval number. From January 1st, 23, all the products of "Yaojianzi" stopped production, and the drug approval document of "National Medicine Zhunzi" will be uniformly adopted. The standardized expression is as follows: the health care drug is "National Medicine Zhunzi B", and the other drugs are: the approval number of chemical drugs is "National Medicine Zhunzi H", the biopharmaceutical "National Medicine Zhunzi S" and the Chinese patent medicine "National Medicine Zhunzi Z".

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Question 5: What do you mean by product specifications of medical devices? Consumables are generally classified into specifications, such as the size of surgical gowns, the capacity of syringes, the thickness of infusion lines, etc., and equipment is generally classified into models.

Question 6: What does it mean to implant medical devices? Hello, let me introduce you to the classification rules of medical devices (Order No.15) (5) Implanting medical devices: any device that enters the human body or natural cavity in whole or in part by means of surgery; These devices are considered as implanted devices if they are left in the body for a long time after the surgical procedure, or if they are partially left in the body for at least 3 days.

If you have time, search the traditional culture forum on Youku. There are many experts there who will give you a lot of useful help in your life!

Question 7: What does MA mean for medical devices? The current that generally appears on X-ray devices and represents X-ray tubes basically represents current on other devices.

Question 8: What does DR mean in medical devices? 1 points depends on which document it appears in. In most cases, DR refers to the digital X-ray imaging system. In addition, DR also refers to the Device R for cord (medical device batch record), and the former is more common.

question 9: I want to know what kind of medical equipment is this? Through the architecture, it can be seen that it is aimed at facial organs, and the specific use is unknown < P > Question 1: What does the medical device promise mean? The medical device license should be the medical device business license.

the establishment of a second-class medical device trading enterprise shall be filed with the people's pharmaceutical supervisory and administrative departments of provinces, autonomous regions and municipalities directly under the central government; The establishment of Class III medical device trading enterprises shall be examined and approved by the people's pharmaceutical supervisory and administrative departments of provinces, autonomous regions and municipalities directly under the Central Government, and a License for Medical Device Trading Enterprises shall be issued.