Taiwan FDA registration 14abf8f93323e1c9e216dfa5b728bdbd

"ALTEOR" Truncal orthosis (Non-Sterile)

TW: "雅第爾" 軀幹裝具 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·ALTEOR·Registered Oct 01, 2021 – Oct 31, 2022Cancelled
Registration details
Analysis ID
14abf8f93323e1c9e216dfa5b728bdbd
License Form
Ministry of Health Medical Device Import Registration No. 017350
Customs Code
DHA08401735006
Company information
Manufacturer
ALTEOR
Manufacturer Country
France
Authorized Representative
MENEY CO., LTD.
Product details
Product Type (Level 1)
o Equipment for physical medicine
Product Type (Level 2)
O3490 Torso Gear
Import Information
Imported from abroad
Dates and status
Registration Date
Oct 01, 2021
Expiry Date
Oct 31, 2022
Cancellation information
Status
Logged out
Reason
未展延而逾期者
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About this record

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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