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"KENDA" Abrasive device and accessories (Non-Sterile) - Taiwan Registration 98718253bcfc8945f8ecc190721cac65

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 98718253bcfc8945f8ecc190721cac65 and manufactured by KENDA AG. The authorized representative in Taiwan is FRANKFURT 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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98718253bcfc8945f8ecc190721cac65
Registration Details
Taiwan FDA Registration: 98718253bcfc8945f8ecc190721cac65
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Device Details

"KENDA" Abrasive device and accessories (Non-Sterile)
TW: "ๅขพ้”" ็ ”็ฃจ่ฃ็ฝฎๅŠๅ…ถ้™„ไปถ (ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

98718253bcfc8945f8ecc190721cac65

Ministry of Health Medical Device Import No. 017886

DHA09401788604

Company Information

Liechtenstein

Product Details

F Dental devices

F6010 Grinding device and accessories

Imported from abroad

Dates and Status

May 24, 2017

May 24, 2022

Cancellation Information

Logged out

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