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"Ankdiant" polisher (unsterilized) - Taiwan Registration 258da4327eb950add04629e1284f3b43

Access comprehensive regulatory information for "Ankdiant" polisher (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 258da4327eb950add04629e1284f3b43 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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258da4327eb950add04629e1284f3b43
Registration Details
Taiwan FDA Registration: 258da4327eb950add04629e1284f3b43
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Device Details

"Ankdiant" polisher (unsterilized)
TW: "ๅฎ‰ๅ…‹ๅ…ธ็‰น" ็ฃจๅ…‰ๅ™จ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

258da4327eb950add04629e1284f3b43

DHA04400176808

Company Information

Germany

Product Details

It is used to polish (remove) the reshaping material and smooth the surface of the retort inside the mouth (e.g. crown).

F Dentistry

F.6010 Abrasive devices and accessories thereof

import

Dates and Status

Nov 07, 2005

Nov 07, 2010

Dec 03, 2012

Cancellation Information

Logged out

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