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"Jintai" torso device (unsterilized) - Taiwan Registration 07539d7f180bb2bab1b85f1862b4b4f8

Access comprehensive regulatory information for "Jintai" torso device (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 07539d7f180bb2bab1b85f1862b4b4f8 and manufactured by NEOPLEX INDUSTRIAL CO., LTD.. The authorized representative in Taiwan is NEOPLEX INDUSTRIAL 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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07539d7f180bb2bab1b85f1862b4b4f8
Registration Details
Taiwan FDA Registration: 07539d7f180bb2bab1b85f1862b4b4f8
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Device Details

"Jintai" torso device (unsterilized)
TW: "้€ฒๆณฐ" ่ป€ๅนน่ฃๅ…ท (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

07539d7f180bb2bab1b85f1862b4b4f8

Company Information

Taiwan, Province of China

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Torso Equipment (O.3490)".

o Physical Medical Sciences

O.3490 Torso mounting

Domestic

Dates and Status

Mar 18, 2014

Mar 18, 2019

Jun 22, 2022

Cancellation Information

Logged out

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