A few days ago, the State Drug Administration issued the document "Notice of the General Department of the State Drug Administration on issuing the 2023 medical device industry standard revision plan project" (the drug Administration comprehensive instrument note [2023] 47), announced the 2023 medical device industry standard revision plan project.

Among them, Henan Chaoya Medical Equipment Co., Ltd. as the lead drafting unit, presided over the development of the enterprise-led standard project - "Far infrared magnetic therapy tape (bag)" (project number: A2023106-T-tj) was successfully selected, serial number 91.

Participating in the formulation of the recommended industry standard are also participating units from all over the country: Tianjin Medical Device Quality Supervision and Inspection Center, Henan Pharmaceutical Medical Device Inspection Institute, Hubei Medical Device Quality Supervision and Inspection Institute, Liaoning Pharmaceutical Evaluation and Inspection Center, Jiangxi Medical Device Testing Center, Jilin Medical Device Inspection and Research Institute, Chongqing Medical Device Quality Inspection Center, Anhui Zhongzhike Standardization Research Institute Co., LTD., Henan Chaoya New Materials Material Co., LTD., Henan Yake testing Technology Co., LTD.