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“Dentis” Cleanlant i-Clean Implant System - Taiwan Registration 19d3296245b97c00d266bf610e663d5b

Access comprehensive regulatory information for “Dentis” Cleanlant i-Clean Implant System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 19d3296245b97c00d266bf610e663d5b and manufactured by Dentis Co., Ltd.. The authorized representative in Taiwan is TAIWAN DENTIS DENTAL TECHNOLOGY 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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19d3296245b97c00d266bf610e663d5b
Registration Details
Taiwan FDA Registration: 19d3296245b97c00d266bf610e663d5b
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Device Details

“Dentis” Cleanlant i-Clean Implant System
TW: “登特司”克林蘭特愛客林牙科植體系統
Risk Class 3
MD

Registration Details

19d3296245b97c00d266bf610e663d5b

Ministry of Health Medical Device Import No. 028387

DHA05602838703

Company Information

Korea, Republic of

Product Details

For details, it is Chinese approved copy of the imitation order

F Dental devices

F3640 Bone explants

Imported from abroad

Dates and Status

Apr 25, 2016

Apr 25, 2026