"ALTEOR" Limb orthosis (Non-Sterile)
- Analysis ID
- a58a5d0c3254b02d3e3269ebc897abb8
- License Form
- Ministry of Health Medical Device Import Registration No. 017349
- Customs Code
- DHA08401734908
- Manufacturer
- ALTEOR
- Manufacturer Country
- France
- Authorized Representative
- MENEY CO., LTD.
- Intended Use
- Limited to the first level recognition range of limb equipment (O.3475) of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- o Equipment for physical medicine
- Product Type (Level 2)
- O3475 Body Equipment
- Import Information
- Imported from abroad
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2023
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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.