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"KENDA" Abrasive device and accessories (Non-Sterile) - Taiwan Registration 572b112ea1e67cd237def2984132716d

Access comprehensive regulatory information for "KENDA" 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 572b112ea1e67cd237def2984132716d and manufactured by KENDA AG. DENTAL MANUFACTURING. The authorized representative in Taiwan is ANDERLY TECHNOLOGY CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including KENDA AG, KENDA AG. DENTAL MANUFACTURING, and 4 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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572b112ea1e67cd237def2984132716d
Registration Details
Taiwan FDA Registration: 572b112ea1e67cd237def2984132716d
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Device Details

"KENDA" Abrasive device and accessories (Non-Sterile)
TW: "ๆ‡‡็ญ”" ็ ”็ฃจ่ฃ็ฝฎๅŠ้™„ไปถ (ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

572b112ea1e67cd237def2984132716d

Ministry of Health Medical Device Import No. 017181

DHA09401718105

Company Information

Liechtenstein

Product Details

F Dental devices

F6010 Grinding device and accessories

Imported from abroad

Dates and Status

Nov 16, 2016

Nov 16, 2021

Cancellation Information

Logged out

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