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“Allard International” External limb prosthetic component (Non-Sterile) - Taiwan Registration 3e02568bebd090cd6594ded7c5ff94d1

Access comprehensive regulatory information for “Allard International” External limb prosthetic component (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 3e02568bebd090cd6594ded7c5ff94d1 and manufactured by ALLARD INTERNATIONAL/Camp Scandinavia AB. The authorized representative in Taiwan is TEH LIN PROSTHETIC & ORTHOPAEDIC INC..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including ALLARD INTERNATIONAL/Camp Scandinavia AB, and 1 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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3e02568bebd090cd6594ded7c5ff94d1
Registration Details
Taiwan FDA Registration: 3e02568bebd090cd6594ded7c5ff94d1
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Device Details

“Allard International” External limb prosthetic component (Non-Sterile)
TW: “爾拉國際”體外肢體義肢用組件(未滅菌)
Risk Class 1
MD

Registration Details

3e02568bebd090cd6594ded7c5ff94d1

Ministry of Health Medical Device Import Registration No. 020806

DHA08402080607

Company Information

Product Details

Limited to the first level recognition range of components for in vitro limb prosthetics (O.3420) of the Measures for the Administration of Medical Devices.

o Equipment for physical medicine

O3420 Components for in vitro limb prosthetics

Imported from abroad

Dates and Status

Oct 01, 2021

Oct 31, 2024

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