Taiwan FDA registration ab47e445da137776ae64e9d9b957fa20

"Dunshi Tianjin Factory" root tube paper needle (unsterilized)

TW: "登士派天津廠" 根管紙針 (未滅菌)

Taiwan·Risk Class 1·Dentsply Dental (TianJin) Co., Ltd.·Registered Dec 17, 2015 – Dec 17, 2020Cancelled

Registration details

Analysis ID: ab47e445da137776ae64e9d9b957fa20
Customs Code: DHA09600259402

Company information

Manufacturer: Dentsply Dental (TianJin) 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: Dec 17, 2015
Expiry Date: Dec 17, 2020
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 "Dunshi Tianjin Factory" 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 ab47e445da137776ae64e9d9b957fa20 and manufactured by Dentsply Dental (TianJin) Co., Ltd.. The authorized representative in Taiwan is Taiwan Branch of American Denspie Co., Ltd.

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