Taiwan FDA registration d0e35c31f8c608f455c4507d88f65f82

"Ikel" limb equipment (unsterilized)

TW: "艾凱爾" 肢體裝具 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·M2 GLOBAL., LTD.·Registered Oct 01, 2021 – Oct 31, 2026Active
Registration details
Analysis ID
d0e35c31f8c608f455c4507d88f65f82
Customs Code
DHA08402247507
Company information
Manufacturer
M2 GLOBAL., LTD.
Manufacturer Country
Viet Nam
Authorized Representative
I CAREMED CO., LTD.
Product details
Intended Use
Limited to the first level recognition range of medical equipment classification and grading management measures limb equipment (O.3475).
Product Type (Level 1)
o Physical Medical Sciences
Product Type (Level 2)
O.3475 Limb fittings
Import Information
import
Dates and status
Registration Date
Oct 01, 2021
Expiry Date
Oct 31, 2026
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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 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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