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"Kaiyang Technology" torso device (unsterilized) - Taiwan Registration 6d1ff868d4730ee0fa990fd3b017fc01

Access comprehensive regulatory information for "Kaiyang Technology" 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 6d1ff868d4730ee0fa990fd3b017fc01 and manufactured by SIN SHI FA ENTERPRISE LIMITED. The authorized representative in Taiwan is MIZAR Co., Ltd..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Kaiyang Technology Co., Ltd.;; Xinshifa Enterprise Co., Ltd, and 1 recent registrations in the same category. 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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6d1ff868d4730ee0fa990fd3b017fc01
Registration Details
Taiwan FDA Registration: 6d1ff868d4730ee0fa990fd3b017fc01
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Device Details

"Kaiyang Technology" torso device (unsterilized)
TW: โ€œ้–‹้™ฝ็ง‘ๆŠ€โ€่ป€ๅนน่ฃๅ…ท (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

6d1ff868d4730ee0fa990fd3b017fc01

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;; Contract manufacturing

Dates and Status

Oct 26, 2020

Oct 26, 2025

Sep 30, 2021

Cancellation Information

Logged out

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