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"Dirkken" Disken Dental Bite Analysis Device (Unsterilized) - Taiwan Registration 4bdb806b9498141d4d07250826f768d6

Access comprehensive regulatory information for "Dirkken" Disken Dental Bite Analysis Device (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 4bdb806b9498141d4d07250826f768d6 and manufactured by TEKSCAN, INC.. The authorized representative in Taiwan is MIDEAL TECHNOLOGY 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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4bdb806b9498141d4d07250826f768d6
Registration Details
Taiwan FDA Registration: 4bdb806b9498141d4d07250826f768d6
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Device Details

"Dirkken" Disken Dental Bite Analysis Device (Unsterilized)
TW: โ€œๅพทๅ…‹ๆ–ฏ่‚ฏโ€็ฌฌๆ–ฏ่‚ฏ็‰™็ง‘ๅ’ฌๅˆๅˆ†ๆž่ฃ็ฝฎ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

4bdb806b9498141d4d07250826f768d6

DHA04400541600

Company Information

United States

Product Details

Limited to the first level recognition range of occlusal paper (F.6140) of the Measures for the Administration of Medical Equipment.

F Dentistry

F.6140 Occlusal paper

import

Dates and Status

Dec 06, 2006

Dec 06, 2011

Nov 26, 2012

Cancellation Information

Logged out

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