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"HDI" Articulation paper (Non-Sterile) - Taiwan Registration db26cbd49387ade4f38052c333354240

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 db26cbd49387ade4f38052c333354240 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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db26cbd49387ade4f38052c333354240
Registration Details
Taiwan FDA Registration: db26cbd49387ade4f38052c333354240
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Device Details

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

Registration Details

db26cbd49387ade4f38052c333354240

Ministry of Health Medical Device Import No. 018513

DHA09401851309

Company Information

Korea, Republic of

Product Details

F Dental devices

F6140 Occlusal paper

Imported from abroad

Dates and Status

Nov 15, 2017

Nov 15, 2022

Cancellation Information

Logged out

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