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"Kende" dental hand instruments (unsterilized) - Taiwan Registration d5339f8b0b3271a189d41caf0bce16db

Access comprehensive regulatory information for "Kende" dental hand instruments (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d5339f8b0b3271a189d41caf0bce16db and manufactured by KETTENBACH GMBH & CO. KG. The authorized representative in Taiwan is YONG CHIEH ENTERPRISE 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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d5339f8b0b3271a189d41caf0bce16db
Registration Details
Taiwan FDA Registration: d5339f8b0b3271a189d41caf0bce16db
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Device Details

"Kende" dental hand instruments (unsterilized)
TW: โ€œ่‚ฏๅพทโ€็‰™็ง‘ๆ‰‹็”จๅ™จๆขฐ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

d5339f8b0b3271a189d41caf0bce16db

DHA04400613701

Company Information

Germany

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Dental Hand Instruments (F.4565)".

F Dentistry

F.4565 ็‰™็ง‘ๆ‰‹็”จๅ™จๆขฐ

import

Dates and Status

Sep 07, 2007

Sep 07, 2012

May 05, 2014

Cancellation Information

Logged out

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