Relevant news shows that under the requirements of the AQSIQ, entry-exit inspection and quarantine institutions across the country are strengthening supervision and management of imported medical devices. The focus of supervision is on two types of products: one is importing unlicensed medical device products, and the other is importing unqualified medical devices. Since the beginning of this year, many local inspection and quarantine departments have investigated and dealt with many imported medical products. Among them, some places have said “no†to relevant imported products for the first time. The latest, Tianjin returned a batch of unlicensed biopsy needles According to the news of the Central Broadcasting Network on July 9, the Tianjin Inspection and Quarantine Department implemented a return shipment treatment for a batch of disposable medical devices originating in Italy. The imported disposable medical devices were biopsy needles, totaling 230 pieces, with a value of 2,783 euros, which did not enter the market. The on-site inspection found that the production date of the batch of biopsy needles was not within the validity period of its Medical Device Registration Certificate, and it was an unlicensed imported product. This is the first time that the Tianjin Airport Inspection and Quarantine Bureau has returned the imported medical device products during the year. The number of returned shipments is rare in recent years. In June, Shandong Heze returned a batch of unlicensed and unqualified color ultrasound The reporter from the Heze Entry and Exit Inspection and Quarantine Bureau was informed that the staff of the bureau recently found that the color ultrasound system was an unqualified imported medical device product when it was inspected for a batch of imported color ultrasonic diagnostic system. The product is returned for processing. It is understood that the batch of unqualified product labels are not factory labels, have been changed, do not meet the requirements of GB 9706.1-2007 "medical electrical equipment part 1 safety general requirements" in the "permanently adhere to" requirements; product display and host system It shows that the model number of the product does not match the model of the cargo inspection material. At the same time, the color ultrasonic diagnostic system of this model is not registered in China, and there is no Medical Device Registration Certificate. In May, Hunan Huaihua returned a unqualified color ultrasound According to the official website of Hunan Entry-Exit Inspection and Quarantine Bureau in late May, Huaihua Inspection and Quarantine Bureau after on-site inspection and evidence collection of an imported color ultrasonic diagnostic system, finally determined that the equipment was unqualified and ordered the applicant to return. This is the first time that the bureau has detected unqualified medical devices and returned them for processing. According to reports, the station imported color ultrasound diagnostic system, model EPIQ 5, serial number US516C0604, the value of 95,000 euros, air transport from Denmark to Changsha Airport, and then shipped to the destination Huaihua. Upon inspection, it was found that the batch of equipment is provided with the Chinese user manual (instruction) without registration certificate number and the name, address and contact information of the agent. The Chinese label (body nameplate) of the equipment has no agent's name, address and contact information. And other relevant content. It has been confirmed by multiple channels that the inspectors cannot complete the legal rectification of the labels and instructions. Food Grade Phosphate,Dimagnesium Phosphate,Iron Pyrophosphate Powder,Ferric Diphosphate Wuxi Yangshan Biochemical Co.,Ltd. , https://www.yangshanchem.com