“Gyrus ACMI” Silicone Single-J Urinary Diversion Stent - Taiwan Registration 9395cbe5b4c2d3ac9fbc00647703e477

Access comprehensive regulatory information for “Gyrus ACMI” Silicone Single-J Urinary Diversion Stent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9395cbe5b4c2d3ac9fbc00647703e477 and manufactured by Gyrus ACMI, Inc.. The authorized representative in Taiwan is YUAN LI INSTRUMENT CO., LTD..

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