Approval number: Yuzheng Food and Drug Administration 5

Batch number and patent number, I have found out where you checked Gu Xintai network customer service told me this**, but this ** can't be not a country? Enter the patent number in the search of the State Intellectual Property Office**, and you can find out.

The State Food and Drug Administration can also inquire, this batch number has been cancelled, I also asked their online sales staff said that as long as it is produced before January 6, 2011, it belongs to the old valid batch number! The new lot number has been approved and the new lot number will be announced! This Guxintai is an external drug, and the batch number classification belongs to the medical device, not the batch number of the internal drug.

Valid until August 31, 2012, but the old batch number and the product are still within the validity range.

This is a fake drug.

I went to the State Food and Drug Administration to check, but the patent number and approval number did not exist.

Article 5 The medical device registration certificate shall be uniformly printed by the State Food and Drug Administration, and the corresponding content shall be filled in by the (food) drug supervision and administration department for approval and registration.

The registration number is arranged in the following way:

1 (Food) Drug Administration (2) Zi 3 No. 4 5 6. Where:

1 is the abbreviation of the location of the registration and approval department:

Domestic Class III medical devices, overseas medical devices, and medical devices in Taiwan, Hong Kong, and Macao are the word "country";

The second class of medical devices in China is the abbreviation of the province, autonomous region and municipality directly under the central government where the registration and approval department is located;

The abbreviation of the province, autonomous region and municipality directly under the Central Government where the registration and approval department is located plus the abbreviation of the administrative area of the city divided into districts is 1 (if there is no corresponding administrative area of the city divided into districts, it is only the abbreviation of the province, autonomous region and municipality directly under the Central Government);

2 is the form of registration (quasi, enter, permit):

The word "quasi" applies to domestic medical devices;

The word "in" applies to overseas medical devices;

The word "Xu" is applicable to medical devices in Taiwan, Hong Kong and Macao;

3 is the year of approval of registration;

4 is the product management category;

5 is the product variety code;

6 is the registration serial number.

Judging from the registration number, this product belongs to a class of medical devices, not drugs.

I just checked it on the website of the State Food and Drug Administration, and sure enough, I found "Yu Food and Drug Administration (Quasi) Zi 2012 No. 2240211".

That's what it says on the Internet:

Production site Zhengzhou High-tech Industrial Development Zone, No. 8 Hehuan West Street Attachment Remarks.

Registration No. 2012 No. 2240211 Production Unit Zhengzhou Forest Medical Equipment****.

Address: Zip code.

Product Name: Laser** Instrument.

Product standard YZB Yu 0016-2012

Product performance structure and composition This product is composed of a controller, a laser coupling line, a laser emitter, a light guide nasal plug, a battery, a charger, a wristband, etc.

Validity Approval Date.

Scope of application of the product It is suitable for the auxiliary of hyperlipidemia, hypertension and hyperglycemia**.

Specifications and models DL-600A, DL-600B, DL-600C Date of change.

It seems to be a bit reliable. But I don't know how effective it is?

You look at whether a product is real or fake, just look at the approval number. Many fake and inferior products are based on the batch numbers of other regular products. However, I didn't find it on the State Food and Drug Administration**, so you can check it yourself.

When this product was sold, the trademark was "Light God Sugar Meter", and the function was also mythical, and it had no effect at all, so you must not be fooled!! I bought one and I don't even have an address to return it!! **！！！

How could it be true? Everyone will understand when you think about Wang Lin's "master".

Device approval document of Shangqiu Food and Drug Administration, Henan Province.

Drug approval number format: Sinopharm quasi-word + 1-digit letter + 8-digit number, trial production drug approval number format: Sinopharm test word + 1-digit letter + 8-digit number.

1) The word "quasi" represents the drugs approved by the state for formal production, and the word "trial" represents the drugs approved by the state for trial production.

2) The 1-digit Chinese pinyin letter after the word "national medicine quasi" (test) represents the drug category, which is H for chemical drugs, S for biological products, J for imported packaged drugs, T for in vitro chemical diagnostic reagents, F for pharmaceutical excipients, B for health care drugs, and Z for traditional Chinese medicine.

3) The first of the 8 Arabic numerals after the Chinese pinyin letter represents the approval of the ** of the document number.

State Food and Drug Administration. It is a medical device approved by the State Food and Drug Administration, which belongs to Class 3 medical devices.

Local approvals, such as the word Yu Food and Drug Administration (quasi), are approved by the Henan Provincial Bureau, and belong to Class 2 or Class 1 medical devices.

The quasi-words in parentheses are domestic. (Enter) refers to imported medical devices, (Xu) refers to Hong Kong, Macao and Taiwan.

Medical devices. Class 3 medical devices and Hong Kong, Macao and Taiwan, imported devices are approved by the State Bureau, you have time to read the "Medical Device Registration Management Measures".

It's clear.

Device approval document of Shangqiu Food and Drug Administration, Henan Province, file number.

You can go to the State Food and Drug Administration to check, and your data information is as follows:

Domestic devices. Registration No.: Yuhua Food and Drug Administration (Quasi) 2012 No. 1640003.

Product name: Nasal carrier fluid antimicrobial.

Production unit: Anyang Bokang medical equipment****.

Address: Shifo Village, Baidaokou Town, Huaxian County.

Product standard YZB Yu (slip) 0003-2012

Product performance structure and composition This product is composed of a reservoir, a sealing ring, a snap-on or screw cap, a nozzle and an outer cap. The carrier liquid is an antibacterial liquid (a compound preparation of dialkyl quaternary ammonium salt and chlorhexidine acetate), which has a killing effect on bacteria, fungi and viruses.

Scope of application of this product is suitable for acute rhinitis, chronic rhinitis, allergic rhinitis, simple rhinitis, hypertrophic rhinitis, sinusitis, caseating rhinitis and other diseases. It can also be used for antimicrobial before and after nasal surgery**.

Specifications and models BQ-10ML, BQ-20ML, BQ-30ML

Date of approval. The date of change of the expiration date.

Production site: Shifo Village, Baidaokou Town, Huaxian County.

Zip code attachment remarks.

Yuslip Food and Drug Administration.

Henan Huaxian County Food and Drug Administration**.

Check the website of the National Food and Drug Administration.

Yuyao word: Z0506328 Such an approval number is the approval number of hospital preparations. It is a traditional Chinese medicine preparation produced by the preparation room of the hospital approved by Henan Province.

According to the provisions of the Drug Administration Law, preparations prepared by medical institutions can be used in the hospital. It cannot be sold in other hospitals or pharmaceutical business enterprises outside of this hospital.

The approval number of the State Food and Drug Administration to approve the production of drugs is: "National Drug Quasi-word H (or digits"), which means that the State Food and Drug Administration approved the production and marketing of drugs, and the letter H represents chemical drugs, Z Chinese patent medicines, S biological products, J imported drugs are packaged in China, and B has the role of assisting and relieving the drug.

There are 2 approval numbers for health food (i.e., health products): 1. The approval number of the State Food and Drug Administration: Guoshijian G (J) plus year number and serial number, and the letter G refers to domestic production J refers to imports.

2. The approval number of the Ministry of Health: Wei Liang Ji Shi Jian Zi (Wei Shi Jian Jin Zi) plus the year number and serial number. It is also stipulated that the special identification of health products must be marked above the packaging or label:

Blue hat", a pattern similar to a blue hat, with the words health food underneath.