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“White Dental” Abrasive Device and Accessories (Non-Sterile) - Taiwan Registration 88c41cecc5cb1c8d3dfb6812c2c08754

Access comprehensive regulatory information for “White Dental” Abrasive Device and Accessories (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 88c41cecc5cb1c8d3dfb6812c2c08754 and manufactured by KENDA AG. The authorized representative in Taiwan is WHITE DENTAL CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including MEDIVANCE INSTRUMENTS LTD, KENDA AG, and 3 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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88c41cecc5cb1c8d3dfb6812c2c08754
Registration Details
Taiwan FDA Registration: 88c41cecc5cb1c8d3dfb6812c2c08754
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Device Details

“White Dental” Abrasive Device and Accessories (Non-Sterile)
TW: “白色牙材”研磨裝置及其附件 (未滅菌)
Risk Class 1
MD
Cancelled

Registration Details

88c41cecc5cb1c8d3dfb6812c2c08754

Ministry of Health Medical Device Import No. 021122

DHA09402112204

Company Information

Liechtenstein

Product Details

F Dental devices

F6010 Grinding device and accessories

Imported from abroad

Dates and Status

Dec 20, 2019

Dec 20, 2024

Cancellation Information

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