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"Baojian" extracorporeal shock wave therapy instrument - Taiwan Registration a5ce1b54481cf90d30905ae474ebcd0d

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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a5ce1b54481cf90d30905ae474ebcd0d
Registration Details
Taiwan FDA Registration: a5ce1b54481cf90d30905ae474ebcd0d
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Device Details

"Baojian" extracorporeal shock wave therapy instrument
TW: โ€œๅฏถๅฅโ€้ซ”ๅค–้œ‡ๆณขๆฒป็™‚ๅ„€
Risk Class 3

Registration Details

a5ce1b54481cf90d30905ae474ebcd0d

DHY00500332907

Company Information

Taiwan, Province of China

Product Details

Plantar fasciitis.

N Orthopedics

N.0001 ้ชจ็ง‘็”จ้ซ”ๅค–้œ‡ๆณข็ณป็ตฑ

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

Jun 20, 2011

Jun 20, 2026