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"ALTEOR" Truncal orthosis (Non-Sterile) - Taiwan Registration 14abf8f93323e1c9e216dfa5b728bdbd

Access comprehensive regulatory information for "ALTEOR" Truncal 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 14abf8f93323e1c9e216dfa5b728bdbd 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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14abf8f93323e1c9e216dfa5b728bdbd
Registration Details
Taiwan FDA Registration: 14abf8f93323e1c9e216dfa5b728bdbd
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Device Details

"ALTEOR" Truncal orthosis (Non-Sterile)
TW: "้›…็ฌฌ็ˆพ" ่ป€ๅนน่ฃๅ…ท (ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

14abf8f93323e1c9e216dfa5b728bdbd

Ministry of Health Medical Device Import Registration No. 017350

DHA08401735006

Company Information

France

Product Details

o Equipment for physical medicine

O3490 Torso Gear

Imported from abroad

Dates and Status

Oct 01, 2021

Oct 31, 2022

Cancellation Information

Logged out

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