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"Bidi I" isokinetic muscle strength test evaluation system - Taiwan Registration f7378fc2e059c758814e221a49e5b082

Access comprehensive regulatory information for "Bidi I" isokinetic muscle strength test evaluation system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f7378fc2e059c758814e221a49e5b082 and manufactured by BTE TECHNOLOGIES, INC.. The authorized representative in Taiwan is WHOLE WELL CO., LTD..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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f7378fc2e059c758814e221a49e5b082
Registration Details
Taiwan FDA Registration: f7378fc2e059c758814e221a49e5b082
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Device Details

"Bidi I" isokinetic muscle strength test evaluation system
TW: โ€œๅฟ…ๅธไธ€โ€็ญ‰้€Ÿ่‚ŒๅŠ›่ฉฆ้ฉ—่ฉ•ไผฐ็ณป็ตฑ
Risk Class 1
Cancelled

Registration Details

f7378fc2e059c758814e221a49e5b082

DHA04400501505

Company Information

United States

Product Details

It is limited to the first level of identification scope of the "Isokinetic Muscle Strength Test Evaluation System (O.1925)" of the Administrative Measures for Medical Devices.

o Physical Medical Sciences

O.1925 ็ญ‰้€Ÿ่‚ŒๅŠ›่ฉฆ้ฉ—่ฉ•ไผฐ็ณป็ตฑ

Input;; QMS/QSD

Dates and Status

Aug 03, 2006

Aug 03, 2011

Jul 25, 2014

Cancellation Information

Logged out

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