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"Aikel" torso device (unsterilized) - Taiwan Registration 3964811819aa365e3d0a44f6464c8c6d

Access comprehensive regulatory information for "Aikel" 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 3964811819aa365e3d0a44f6464c8c6d and manufactured by SIN SHI FA ENTERPRISE LIMITED. The authorized representative in Taiwan is I CAREMED CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including SIN SHI FA ENTERPRISE LIMITED, Aikel Medical Devices Co., Ltd.;; Xinsifa Enterprises Limited, and 2 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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3964811819aa365e3d0a44f6464c8c6d
Registration Details
Taiwan FDA Registration: 3964811819aa365e3d0a44f6464c8c6d
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Device Details

"Aikel" torso device (unsterilized)
TW: "่‰พๅ‡ฑ็ˆพ" ่ป€ๅนน่ฃๅ…ท (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

3964811819aa365e3d0a44f6464c8c6d

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

Sep 04, 2019

Sep 04, 2024

Sep 30, 2021

Cancellation Information

Logged out

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