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Anchor Tec grinding device and its accessories (unsterilized) - Taiwan Registration 98cc1b7036ef9ff2f400c8f41102302d

Access comprehensive regulatory information for Anchor Tec grinding device and its accessories (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 98cc1b7036ef9ff2f400c8f41102302d and manufactured by MK-DENT GMBH. The authorized representative in Taiwan is LI-XIANG INTERNATIONAL 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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98cc1b7036ef9ff2f400c8f41102302d
Registration Details
Taiwan FDA Registration: 98cc1b7036ef9ff2f400c8f41102302d
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Device Details

Anchor Tec grinding device and its accessories (unsterilized)
TW: โ€œๅฎ‰ๅ…‹ๅ…ธ็‰นโ€็ ”็ฃจ่ฃ็ฝฎๅŠๅ…ถ้™„ไปถ๏ผˆๆœชๆป…่Œ๏ผ‰
Risk Class 1
Cancelled

Registration Details

98cc1b7036ef9ff2f400c8f41102302d

DHA04400954900

Company Information

Germany

Product Details

Limited to the first level identification range of grinding devices and their accessories (F.6010) under the management measures for medical equipment.

F Dentistry

F.6010 Abrasive devices and accessories thereof

import

Dates and Status

Nov 22, 2010

Nov 22, 2025

Sep 30, 2021

Cancellation Information

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