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"Ikel" limb equipment (unsterilized) - Taiwan Registration 3f5a77f44a729b6621f4b8987c4e982a

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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3f5a77f44a729b6621f4b8987c4e982a
Registration Details
Taiwan FDA Registration: 3f5a77f44a729b6621f4b8987c4e982a
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Device Details

"Ikel" limb equipment (unsterilized)
TW: "่‰พๅ‡ฑ็ˆพ" ่‚ข้ซ”่ฃๅ…ท (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

3f5a77f44a729b6621f4b8987c4e982a

Company Information

Taiwan, Province of China

Product Details

Limited to the first level recognition range of limb equipment (O.3475) of the Measures for the Administration of Medical Devices.

o Physical Medical Sciences

O.3475 Limb fittings

Contract manufacturing;; Domestic

Dates and Status

Sep 04, 2019

Sep 04, 2024

Sep 30, 2021

Cancellation Information

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