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"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.

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d43fb319290a67fea29f5ba436f3e6a1
Registration Details
Taiwan FDA Registration: d43fb319290a67fea29f5ba436f3e6a1
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Device Details

"HDI" Articulation paper (Non-Sterile)
TW: "่‰พๅ–ๅพท" ๅ’ฌๅˆ็ด™ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

d43fb319290a67fea29f5ba436f3e6a1

Ministry of Health Medical Device Import Registration No. 018513

DHA08401851300

Company Information

Korea, Republic of

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

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