“Cordis” Sleek Percutaneous Transluminal Angioplasty (PTA) Catheter - Taiwan Registration 5deb8ddc5d87c52bb66892e6a29785ab

Access comprehensive regulatory information for “Cordis” Sleek Percutaneous Transluminal Angioplasty (PTA) Catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5deb8ddc5d87c52bb66892e6a29785ab and manufactured by CLEARSTREAM TECHNOLOGIES LTD.. The authorized representative in Taiwan is EMERGO TAIWAN LIMITED.

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