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Aesthetic Syringe And Solid Connector Industry Standards Are Different To Lead To Confusion
Dr.c | Updated: Oct 16, 2017

Aesthetic Syringe And Solid Connector industry standards are different to lead to confusion
As a result of the Aesthetic Syringe And Solid Connector regulatory authorities on the "Aesthetic Syringe And Solid Connector classification rules" in the degree of awareness and grasp the scale is different, resulting in Aesthetic Syringe And Solid Connector new product registration category in practice there are many problems. Mainly in the following areas:
1.Aesthetic Syringe And Solid Connector is not confused with non-Aesthetic Syringe And Solid Connector. The same product is identified as Aesthetic Syringe And Solid Connector in one place and in another where it is considered a non-Aesthetic Syringe And Solid Connector;
2. Management category is not uniform. The same Aesthetic Syringe And Solid Connector product was identified as the first category Aesthetic Syringe And Solid Connector in one place, and in the other was identified as the second category Aesthetic Syringe And Solid Connector;
3. Class code is inconsistent. The same product, in one place, is identified as this type of code, and in another is identified as another class code.
The existence of these problems, undermined the Aesthetic Syringe And Solid Connector product registration seriousness, but also to Aesthetic Syringe And Solid Connector market regulation has brought many difficulties.
In order to maintain the seriousness of the registration of the Aesthetic Syringe And Solid Connector, maintain the authority of the Aesthetic Syringe And Solid Connector. The author believes that Aesthetic Syringe And Solid Connector is required to set up a new product registration category. I suggest that Aesthetic Syringe And Solid Connector to determine the type of new product registration should be carried out as follows:
First of all, all Aesthetic Syringe And Solid Connector new and new product registration category, whether it is the first category or the second category and even the third category of products, unified by the provincial food and drug regulatory authorities to review and determine the production enterprises to the corresponding Proof, at the same time to the State Food and Drug Administration for the record.
Second, by the manufacturer according to the provincial regulatory authorities issued a certificate to the corresponding Aesthetic Syringe And Solid Connector regulatory authorities to declare Aesthetic Syringe And Solid Connector registration procedures. The provincial regulatory authorities that is the first category Aesthetic Syringe And Solid Connector, the enterprise to the corresponding municipal regulatory authorities to declare the registration; is the second category Aesthetic Syringe And Solid Connector, the enterprise to the provincial management department to declare registration; Three types of Aesthetic Syringe And Solid Connector, the enterprise to the State Food and Drug Administration to declare the registration.
Once again, if a Aesthetic Syringe And Solid Connector product is recognized by the provincial regulatory authorities as the third category, and the enterprise to the State Food and Drug Administration to declare, the National Bureau that the product for the second category or the first category of products, then By the national bureau issued by the corresponding proof, by the enterprise to prove to the corresponding regulatory authorities to declare the registration.
Finally, when the National Bureau examines the filing materials of the provincial regulatory authorities, if the management category identified by the provincial regulatory authorities is considered to be incorrect, it can be adjusted in the corresponding classification of the document, but the previously registered product is still valid until When the product is re-registered, the manufacturer will then adjust it according to the new management category stipulated by the National Bureau.
However, the person also mentioned that although China's current level of independent innovation is not enough, but even imitation of foreign products, domestic equipment also has a vast space. Now more and more attention to product quality, domestic equipment, the level of technology is also getting higher and higher, these highly cost-effective products make import substitution become a trend.
On the other hand, China Aesthetic Syringe And Solid Connector concentration is generally low, has not yet formed a scale effect. As of the end of 2012, China Aesthetic Syringe And Solid Connector production enterprises have reached 17.78 million, about 90% of Aesthetic Syringe And Solid Connector production enterprises in the annual income of less than 20 million low production technology in small and medium enterprises. The production of electronic monitoring equipment, ultrasound diagnostic equipment, ECG physiological equipment, X-ray tomography equipment, CT and other high-tech products with independent brands and income scale of more than 500 million enterprises are not many. Which makes the ability of enterprises and hospitals to negotiate lower.
However, this situation is slowly changing, in recent years, the rapid development of the advantages of capital companies are mergers and acquisitions, etc., continue to expand the scale to enhance the brand effect, is expected to China Aesthetic Syringe And Solid Connector industry consolidation will continue.

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