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"HOKOMA" isokinetic strength test evaluation system (unsterilized) - Taiwan Registration a970867bebc678ea458822a4bb96e353

Access comprehensive regulatory information for "HOKOMA" isokinetic strength test evaluation system (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a970867bebc678ea458822a4bb96e353 and manufactured by HOCOMA AT. The authorized representative in Taiwan is AMPLE MEDICAL INSTRUMENTS 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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a970867bebc678ea458822a4bb96e353
Registration Details
Taiwan FDA Registration: a970867bebc678ea458822a4bb96e353
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Device Details

"HOKOMA" isokinetic strength test evaluation system (unsterilized)
TW: โ€œ่ณ€ๅฏ็‘ชโ€ ็ญ‰้€Ÿ่‚ŒๅŠ›่ฉฆ้ฉ—่ฉ•ไผฐ็ณป็ตฑ(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

a970867bebc678ea458822a4bb96e353

DHA04401132608

Company Information

Switzerland

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Isokinetic Muscle Strength Test Evaluation System (O.1925)".

o Physical Medical Sciences

O.1925 ็ญ‰้€Ÿ่‚ŒๅŠ›่ฉฆ้ฉ—่ฉ•ไผฐ็ณป็ตฑ

Input;; QMS/QSD

Dates and Status

Jan 31, 2012

Jan 31, 2017

Nov 26, 2019

Cancellation Information

Logged out

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