"HDI" Articulation paper (Non-Sterile) - Taiwan Registration d43fb319290a67fea29f5ba436f3e6a1
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.
Device Details
Registration Details
d43fb319290a67fea29f5ba436f3e6a1
Ministry of Health Medical Device Import Registration No. 018513
DHA08401851300
Product Details
Limited to the first level recognition range of occlusal paper (F.6140) of the Measures for the Administration of Medical Equipment.
F Dental devices
F6140 Occlusal paper
Imported from abroad
Dates and Status
Oct 01, 2021
Oct 31, 2023

