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"Testisi" impression mixer (unsterilized) - Taiwan Registration ff612e4feb7aadbc85c7cb869999e984

Access comprehensive regulatory information for "Testisi" impression mixer (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number ff612e4feb7aadbc85c7cb869999e984 and manufactured by TPC ADVANCED TECHNOLOGIES, INC.. The authorized representative in Taiwan is TE CHANG MEDICAL INSTRUMENT CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including TPC ADVANCED TECHNOLOGIES, INC., and 1 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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ff612e4feb7aadbc85c7cb869999e984
Registration Details
Taiwan FDA Registration: ff612e4feb7aadbc85c7cb869999e984
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Device Details

"Testisi" impression mixer (unsterilized)
TW: โ€œ็‰นๆฏ”่ฅฟโ€ๅฐๆจกๆททๅˆ็ฎก (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

ff612e4feb7aadbc85c7cb869999e984

DHA04400799408

Company Information

United States

Product Details

Limited to the first-level identification range of the Measures for the Administration of Medical Equipment "Impression Tube (F.6570)".

F Dentistry

F.6570 Impression tubes

import

Dates and Status

Aug 25, 2009

Aug 25, 2024

Sep 30, 2021

Cancellation Information

Logged out

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