Product model: zs01
Specifications:
1ml, 2ml, 2.5ml, 3ml, 5ml, 10ml, 20ml, 30ml, 50ml, 60ml, 100ml
THREE-PART LUER SLIP SYRINGE FOR SINGLE USE
News Information
20 kinds of medical devices are unqualified
- Categories:Industry News
- Time of issue:2015-07-31 08:15
(Summary description)The State Food and Drug Administration issued a national medical device quality announcement yesterday. After random inspections of 476 batches (sets) of 21 varieties of medical device products including semiconductor laser treatment machines and electric suction devices, it was found that 56 batches (sets) of 20 varieties did not meet the standard requirements, involving 48 manufacturing companies. The specific list has been published on the website of the State Food and Drug Administration. At present, the local food and drug regulatory authorities have issued warnings, ordered suspension of production and business, confiscation of products and illegal income, administrative fines and other administrative penalties for product manufacturers that do not meet the standards. The Food and Drug Administration requires the companies involved to find out the reasons, formulate rectification measures and rectify them within a time limit, and announce the relevant handling conditions to the public.
20 kinds of medical devices are unqualified
(Summary description)The State Food and Drug Administration issued a national medical device quality announcement yesterday. After random inspections of 476 batches (sets) of 21 varieties of medical device products including semiconductor laser treatment machines and electric suction devices, it was found that 56 batches (sets) of 20 varieties did not meet the standard requirements, involving 48 manufacturing companies. The specific list has been published on the website of the State Food and Drug Administration. At present, the local food and drug regulatory authorities have issued warnings, ordered suspension of production and business, confiscation of products and illegal income, administrative fines and other administrative penalties for product manufacturers that do not meet the standards. The Food and Drug Administration requires the companies involved to find out the reasons, formulate rectification measures and rectify them within a time limit, and announce the relevant handling conditions to the public.
- Categories:Industry News
- Time of issue:2015-07-31 08:15
- Views:
Information
The State Food and Drug Administration issued a national medical device quality announcement yesterday. After random inspections of 476 batches (sets) of 21 varieties of medical device products including semiconductor laser treatment machines and electric suction devices, it was found that 56 batches (sets) of 20 varieties did not meet the standard requirements, involving 48 manufacturing companies. The specific list has been published on the website of the State Food and Drug Administration. At present, the local food and drug regulatory authorities have issued warnings, ordered suspension of production and business, confiscation of products and illegal income, administrative fines and other administrative penalties for product manufacturers that do not meet the standards. The Food and Drug Administration requires the companies involved to find out the reasons, formulate rectification measures and rectify them within a time limit, and announce the relevant handling conditions to the public.
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Jiangsu Kanghua Medical Equipment Co., Ltd.
Focus on the production and sales of disposable medical devices and large infusion medicine packages.
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