Acotec Scientific Holdings Ltd. Secures PRC National Medical Products Administration Approval for E-Peridge® Peripheral Scoring Balloon Dilatation Catheter

Reuters
05-29
Acotec Scientific Holdings Ltd. Secures PRC National Medical Products Administration Approval for E-Peridge® Peripheral Scoring Balloon Dilatation Catheter

Acotec Scientific Holdings Ltd. has announced that it has received registration approval from the PRC National Medical Products Administration for its Peripheral Scoring Balloon Dilatation Catheter, E-Peridge®. This approval, granted on May 27, 2025, marks a significant milestone for the company as it enhances its product portfolio aimed at treating stenotic lesions in peripheral vessels, including the iliac and renal arteries. The E-Peridge® catheter is designed to provide effective anchoring and reduce elastic recoil of plaques, thus minimizing vascular injury. Acotec plans to initiate marketing activities in the PRC market, although the company cautions that successful commercialization is not guaranteed.

Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Acotec Scientific Holdings Ltd. published the original content used to generate this news brief on May 29, 2025, and is solely responsible for the information contained therein.

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