NEWS
23
2022-03
"Measures for the Supervision and Administration of Medical Device Production" (Order No. 53 of the State Administration for Market Regulation) (hereinafter referred to as the "Production Measures") "Measures for the Supervision and Administration of Medical Device Operation" (Order No. 54 of the State Administration for Market Regulation) (hereinafter referred to as the "Measures for the Supervision and Administration of Medical Devices" (Order No. 54 of the State Administration for Market Regulation) Operational Measures") has been issued and will come into force on May 1, 2022.
2022-03-23
10
2022-03
Measures for the Supervision and Administration of Medical Device Production
In order to strengthen the supervision and management of medical device production, standardize medical device production activities, and ensure the safety and effectiveness of medical devices, these Measures are formulated in accordance with the Regulations on the Supervision and Administration of Medical Devices.
2022-03-10
01
2016-08
Jiangsu Province Safety Production Regulations
In order to strengthen production safety work, prevent and reduce production safety accidents, protect people's lives and property safety, and promote sustainable and healthy economic and social development, these Regulations are formulated in accordance with the "Safety Production Law of the People's Republic of China" and other laws and administrative regulations and in light of the actual conditions of this province. .
2016-08-01
30
2021-06
Adopted at the 28th meeting of the Standing Committee of the Ninth National People's Congress on June 29, 2002 in accordance with the 10th meeting of the Standing Committee of the Eleventh National People's Congress on August 27, 2009 "On Amending Some Laws" The first amendment of the Decision is based on the Decision on Amending the Work Safety Law of the People's Republic of China at the Tenth Meeting of the Standing Committee of the Twelfth National People's Congress on August 31, 2014. The second amendment is based on June 2021. On the 10th, the 29th meeting of the Standing Committee of the 13th National People's Congress "Decision on Amending the "Production Safety Law of the People's Republic of China" was revised for the third time
2021-06-30
01
2022-04
01
2022-04
The company's global portal 2022 version (standard version) website was officially launched
In March 2022, China Enterprise Power, a pioneer in building a domestic website, assisted Nantong Aohua Medical Supplies Co., Ltd. to upgrade and build the website. The design layout and functional sections of the entire page are more in line with the concept of green and healthy development and sustainable management of medical devices.
2022-04-01
24
2014-11
2014 Spring Medical Equipment Expo (Shenzhen)
2014 Spring Medical Equipment Expo (Shenzhen)
2014-11-24
05
2015-01
Qualification requirements: (1) Manufacturers of medical consumables should obtain the "Business License" and "Medical Device Production License" in accordance with the law. Manufacturers of test reagents shall have corresponding production qualifications in accordance with national regulations on in vitro diagnostic reagents. Manufacturers of disinfectants shall obtain a Sanitary License in accordance with the law. (2) Good business reputation. (3) It has the ability to guarantee the supply of medical consumables and testing reagents necessary for the performance of the contract. (4) Have a good record of paying taxes according to law. (5) In the two years before participating in the centralized procurement activities, there is no serious illegal record in the business activities. (6) Supplier qualification organized by service agencies
2015-01-05
10
2015-07
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