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"Ikel" limb equipment (unsterilized) - Taiwan Registration d0e35c31f8c608f455c4507d88f65f82

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 d0e35c31f8c608f455c4507d88f65f82 and manufactured by M2 GLOBAL., LTD.. 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 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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d0e35c31f8c608f455c4507d88f65f82
Registration Details
Taiwan FDA Registration: d0e35c31f8c608f455c4507d88f65f82
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Device Details

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

Registration Details

d0e35c31f8c608f455c4507d88f65f82

DHA08402247507

Company Information

Viet Nam

Product Details

Limited to the first level recognition range of medical equipment classification and grading management measures limb equipment (O.3475).

o Physical Medical Sciences

O.3475 Limb fittings

import

Dates and Status

Oct 01, 2021

Oct 31, 2026