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"Dunshpie" Dregan tube paper needle (unsterilized) - Taiwan Registration 45d2d997c2c59450847a4b5e1e6fdfe3

Access comprehensive regulatory information for "Dunshpie" Dregan 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 45d2d997c2c59450847a4b5e1e6fdfe3 and manufactured by DENTSPLY DENTAL (TIANJIN) 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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45d2d997c2c59450847a4b5e1e6fdfe3
Registration Details
Taiwan FDA Registration: 45d2d997c2c59450847a4b5e1e6fdfe3
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Device Details

"Dunshpie" Dregan tube paper needle (unsterilized)
TW: "็™ปๅฃซๆดพ" ๅพท็‘žๆ น็ฎก็ด™้‡ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

45d2d997c2c59450847a4b5e1e6fdfe3

DHA04600054104

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

Jul 23, 2008

Jul 23, 2018

Jul 15, 2022

Cancellation Information

Logged out

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