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"Dunshpie" root tube paper needle (unsterilized) - Taiwan Registration 04ca7e1de92d311ecb39d985d9e89761

Access comprehensive regulatory information for "Dunshpie" root tube paper needle (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 04ca7e1de92d311ecb39d985d9e89761 and manufactured by TIANJIN GOLDEN VENDOR TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is Taiwan Branch of American Denspie 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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04ca7e1de92d311ecb39d985d9e89761
Registration Details
Taiwan FDA Registration: 04ca7e1de92d311ecb39d985d9e89761
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Device Details

"Dunshpie" root tube paper needle (unsterilized)
TW: "็™ปๅฃซๆดพ" ๆ น็ฎก็ด™้‡ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

04ca7e1de92d311ecb39d985d9e89761

DHA09600226904

Company Information

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices "Root Canal Paper Needle (F.3830)".

F Dentistry

F.3830 Root Canal

Input;; Chinese goods

Dates and Status

Nov 14, 2014

Nov 14, 2019

Jul 15, 2022

Cancellation Information

Logged out

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