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Kenda Abrasive Series (Unsterilized) - Taiwan Registration 4509d215b41dfcd04aaebc2001a23413

Access comprehensive regulatory information for Kenda Abrasive Series (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 4509d215b41dfcd04aaebc2001a23413 and manufactured by KENDA AG. The authorized representative in Taiwan is Sanye Limited.

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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4509d215b41dfcd04aaebc2001a23413
Registration Details
Taiwan FDA Registration: 4509d215b41dfcd04aaebc2001a23413
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Device Details

Kenda Abrasive Series (Unsterilized)
TW: ่‚ฏ้”็ ”็ฃจๆ็ณปๅˆ— (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

4509d215b41dfcd04aaebc2001a23413

DHA04400349802

Company Information

Liechtenstein

Product Details

It is limited to the first level of identification of the Administrative Measures for Medical Devices (Grinding Devices and Their Annexes [F.6010]).

F Dentistry

import

Dates and Status

Apr 07, 2006

Apr 07, 2011

Jan 17, 2013

Cancellation Information

Logged out

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