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"Keystone" Surgical Guide (Non-Sterile) - Taiwan Registration bd0748cdeaa5edf586443629b2d27fc1

Access comprehensive regulatory information for "Keystone" Surgical Guide (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 bd0748cdeaa5edf586443629b2d27fc1 and manufactured by KEYSTONE DENTAL, INC.. The authorized representative in Taiwan is HUNG KUO MEDICAL INSTRUMENT CO., LTD..

This page provides complete technical specifications, regulatory compliance details. 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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bd0748cdeaa5edf586443629b2d27fc1
Registration Details
Taiwan FDA Registration: bd0748cdeaa5edf586443629b2d27fc1
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Device Details

"Keystone" Surgical Guide (Non-Sterile)
TW: "้‡‘็Ÿณ"ๆ‰‹่ก“ๅฐŽๆฟ(ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

bd0748cdeaa5edf586443629b2d27fc1

Ministry of Health Medical Device Import No. 018563

DHA09401856301

Company Information

United States

Product Details

F Dental devices

F3980 Dental Intraosseous Implant Attachment

Imported from abroad

Dates and Status

Nov 30, 2017

Nov 30, 2022

May 12, 2020

Cancellation Information

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