Taiwan FDA registration 3f5a77f44a729b6621f4b8987c4e982a

"Ikel" limb equipment (unsterilized)

TW: "艾凱爾" 肢體裝具 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·SIN SHI FA ENTERPRISE LIMITED·Registered Sep 04, 2019 – Sep 04, 2024Cancelled
Registration details
Analysis ID
3f5a77f44a729b6621f4b8987c4e982a
Company information
Manufacturer Country
Taiwan, Province of China
Authorized Representative
I CAREMED CO., LTD.
Product details
Intended Use
Limited to the first level recognition range of limb equipment (O.3475) of the Measures for the Administration of Medical Devices.
Product Type (Level 1)
o Physical Medical Sciences
Product Type (Level 2)
O.3475 Limb fittings
Import Information
Contract manufacturing;; Domestic
Dates and status
Registration Date
Sep 04, 2019
Expiry Date
Sep 04, 2024
Cancellation Date
Sep 30, 2021
Cancellation information
Status
Logged out
Reason
轉為登錄字號
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About this record

Access comprehensive regulatory information for "Ikel" limb equipment (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 3f5a77f44a729b6621f4b8987c4e982a 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, 3 companies making similar products including M2 GLOBAL., LTD., Aikel Medical Devices Co., Ltd.;; Xinsifa Enterprises Limited, and 3 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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