“Seawon” Claudicare Percutaneous Endoscopic Neurolysis and Foraminoplasty System - Taiwan Registration a28dc25452477a1257a6f2e5eeef1670

Access comprehensive regulatory information for “Seawon” Claudicare Percutaneous Endoscopic Neurolysis and Foraminoplasty System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a28dc25452477a1257a6f2e5eeef1670 and manufactured by Seawon Meditech Co., Ltd.. The authorized representative in Taiwan is BUTICON INTERNATIONAL CORPORATION.

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