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"Aikel" torso device (unsterilized) - Taiwan Registration 065e37590d1744e16631259355e2ff69

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 065e37590d1744e16631259355e2ff69 and manufactured by Aikel Medical Devices Co., Ltd.;; Xinsifa Enterprises Limited. The authorized representative in Taiwan is I CAREMED CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including SIN SHI FA ENTERPRISE 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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065e37590d1744e16631259355e2ff69
Registration Details
Taiwan FDA Registration: 065e37590d1744e16631259355e2ff69
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Device Details

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

Registration Details

065e37590d1744e16631259355e2ff69

Company Information

Product Details

Limited to the first level identification scope of the "Torso Equipment (O.3490)" classification and grading management measures for medical equipment.

o Physical Medical Sciences

O.3490 Torso mounting

Contract manufacturing;; Domestic

Dates and Status

Oct 01, 2021

Oct 31, 2025

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