Taiwan FDA registration a5ce1b54481cf90d30905ae474ebcd0d

"Baojian" extracorporeal shock wave therapy instrument

TW: “寶健”體外震波治療儀

Taiwan·Risk Class 3·Baojian Technology Co., Ltd. new store second factory·Registered Jun 20, 2011 – Jun 20, 2026Expired

Registration details

Analysis ID: a5ce1b54481cf90d30905ae474ebcd0d
Customs Code: DHY00500332907

Company information

Manufacturer: Baojian Technology Co., Ltd. new store second factory
Manufacturer Country: Taiwan, Province of China
Authorized Representative: LITE-MED INC.

Product details

Intended Use: Plantar fasciitis.
Product Type (Level 1): N Orthopedics
Product Type (Level 2): N.0001 骨科用體外震波系統
Import Information: Domestic;; The use of this device shall comply with the provisions of the Administrative Measures for the Implementation or Use of Medical Devices for Specific Medical Technology Inspection and Testing.

Dates and status

Registration Date: Jun 20, 2011
Expiry Date: Jun 20, 2026

About this record

Access comprehensive regulatory information for "Baojian" extracorporeal shock wave therapy instrument in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number a5ce1b54481cf90d30905ae474ebcd0d and manufactured by Baojian Technology Co., Ltd. new store second factory. The authorized representative in Taiwan is LITE-MED INC..

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