"ALTEOR" Limb orthosis (Non-Sterile)
Taiwan·Risk Class 1·MD·ALTEOR·Registered Dec 30, 2016 – Dec 30, 2021Cancelled- Analysis ID
- d79c818b0d63dd8bb94fcbfdccf26bc8
- License Form
- Ministry of Health Medical Device Import No. 017349
- Customs Code
- DHA09401734904
- Manufacturer
- ALTEOR
- Manufacturer Country
- France
- Authorized Representative
- MENEY CO., LTD.
- Product Type (Level 1)
- o Equipment for physical medicine
- Product Type (Level 2)
- O3475 Body Equipment
- Import Information
- Imported from abroad
- Registration Date
- Dec 30, 2016
- Expiry Date
- Dec 30, 2021
- Status
- Logged out
- Reason
- 轉為登錄字號
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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 d79c818b0d63dd8bb94fcbfdccf26bc8 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.