"HDI" Articulation paper (Non-Sterile)
Taiwan·Risk Class 1·MD·HDI INC.·Registered Oct 01, 2021 – Oct 31, 2023Expired- Analysis ID
- d43fb319290a67fea29f5ba436f3e6a1
- License Form
- Ministry of Health Medical Device Import Registration No. 018513
- Customs Code
- DHA08401851300
- Manufacturer
- HDI INC.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- MNM BIOTECHNOLOGY CO., LTD
- Intended Use
- Limited to the first level recognition range of occlusal paper (F.6140) of the Measures for the Administration of Medical Equipment.
- Product Type (Level 1)
- F Dental devices
- Product Type (Level 2)
- F6140 Occlusal paper
- Import Information
- Imported from abroad
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2023
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Access comprehensive regulatory information for "HDI" Articulation paper (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 d43fb319290a67fea29f5ba436f3e6a1 and manufactured by HDI INC.. The authorized representative in Taiwan is MNM BIOTECHNOLOGY CO., LTD.
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including HDI INC., 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.