Taiwan FDA registration 04ca7e1de92d311ecb39d985d9e89761

"Dunshpie" root tube paper needle (unsterilized)

TW: "登士派" 根管紙針 (未滅菌)

Taiwan·Risk Class 1·TIANJIN GOLDEN VENDOR TECHNOLOGY CO., LTD.·Registered Nov 14, 2014 – Nov 14, 2019Cancelled

Registration details

Analysis ID: 04ca7e1de92d311ecb39d985d9e89761
Customs Code: DHA09600226904

Company information

Manufacturer: TIANJIN GOLDEN VENDOR TECHNOLOGY CO., LTD.
Manufacturer Country: China
Authorized Representative: Taiwan Branch of American Denspie Co., Ltd

Product details

Intended Use: Limited to the first level identification range of the Measures for the Administration of Medical Devices "Root Canal Paper Needle (F.3830)".
Product Type (Level 1): F Dentistry
Product Type (Level 2): F.3830 Root Canal
Import Information: Input;; Chinese goods

Dates and status

Registration Date: Nov 14, 2014
Expiry Date: Nov 14, 2019
Cancellation Date: Jul 15, 2022

Cancellation information

Status: Logged out
Reason: 未展延而逾期者

About this record

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.

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