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"ALTEOR" Limb orthosis (Non-Sterile) - Taiwan Registration a58a5d0c3254b02d3e3269ebc897abb8

Access comprehensive regulatory information for "ALTEOR" Limb orthosis (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 a58a5d0c3254b02d3e3269ebc897abb8 and manufactured by ALTEOR. The authorized representative in Taiwan is MENEY CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including ALTEOR, 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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a58a5d0c3254b02d3e3269ebc897abb8
Registration Details
Taiwan FDA Registration: a58a5d0c3254b02d3e3269ebc897abb8
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Device Details

"ALTEOR" Limb orthosis (Non-Sterile)
TW: "้›…็ฌฌ็ˆพ" ่‚ข้ซ”่ฃๅ…ท (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

a58a5d0c3254b02d3e3269ebc897abb8

Ministry of Health Medical Device Import Registration No. 017349

DHA08401734908

Company Information

France

Product Details

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

o Equipment for physical medicine

O3475 Body Equipment

Imported from abroad

Dates and Status

Oct 01, 2021

Oct 31, 2023

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