Diving Medical 2 batch electronic sphygmomanometer sampling failed

On November 24, the Beijing Food and Drug Administration issued a message saying that in the recent medical device sampling, it was found that the two batches of electronic sphygmomanometers produced by Jiangsu Yuyue Medical Equipment Co., Ltd. were unqualified and fined 4 Ten thousand yuan.

Recently, in order to strengthen the supervision and management of medical device quality and ensure the safe and effective use of medical device products, the State Food and Drug Administration has organized the extracorporeal blood circulation of medical protective clothing, non-invasive automatic blood pressure monitor (electronic blood pressure monitor) and blood purification device. The products of 193 batches (Taiwan) were tested for quality supervision.

The sampling inspection found that up to now, two batches of medical device product inspection projects involving two medical device operators in Beijing did not meet the standards. The two batches of medical device products are all electronic sphygmomanometers produced by Jiangsu Yuyue Medical Equipment Co., Ltd., and the unqualified items are not in compliance with the relevant regulations.

Diving Medical 2 batch electronic sphygmomanometer sampling failed

The Beijing Food and Drug Administration has filed an investigation into the relevant enterprises suspected of operating unqualified products in accordance with the "Regulations on the Supervision and Administration of Medical Devices" and other relevant regulations, and has imposed administrative penalties for administrative fines.

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