Taiwan FDA registration 08ae16ae306af7e1999e8f9c95cac157

"Aikel" torso device (unsterilized)

TW: "艾凱爾" 軀幹裝具 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·SIN SHI FA ENTERPRISE LIMITED·Registered May 30, 2014 – May 30, 2019Cancelled
Registration details
Analysis ID
08ae16ae306af7e1999e8f9c95cac157
Company information
Manufacturer Country
Taiwan, Province of China
Authorized Representative
I CAREMED CO., LTD.
Product details
Intended Use
Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Torso Equipment (O.3490)".
Product Type (Level 1)
o Physical Medical Sciences
Product Type (Level 2)
O.3490 Torso mounting
Import Information
Contract manufacturing;; Domestic
Dates and status
Registration Date
May 30, 2014
Expiry Date
May 30, 2019
Cancellation Date
Jun 07, 2022
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
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About this record

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 08ae16ae306af7e1999e8f9c95cac157 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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