The State Drug Administration issued a notice on the cancellation of the Peripheral Adjustable Curved Guide Tube Medical Device Registration Certificate. After investigation, Kang Weining Medical Technology Co., Ltd. provided false information when registering the “Peripheral Adjustable Curved Guide Tube” medical device. According to the provisions of Article 83 of the “Medical Device Supervision and Administration Regulations”, it was decided to withdraw the registration certificate of Kang Weining Medical Technology Co., Ltd.'s peripheral adjustable curved guide tube registration certificate.

The State Drug Administration issued a notice on the cancellation of the Peripheral Adjustable Curved Guide Tube Medical Device Registration Certificate. After investigation, Kang Weining Medical Technology Co., Ltd. provided false information when registering the “Peripheral Adjustable Curved Guide Tube” medical device. According to the provisions of Article 83 of the “Medical Device Supervision and Administration Regulations”, it was decided to withdraw the registration certificate of Kang Weining Medical Technology Co., Ltd.'s peripheral adjustable curved guide tube registration certificate.