Taiwan FDA registration c78271a99113c955ecad448bd9b0998a

"Delden" Root Tube Paper Needle (Sterilized)

TW: "戴爾登" 根管紙針 (滅菌)

Taiwan·Risk Class 1·DIADENT GROUP INTERNATIONAL·Registered May 03, 2024 – May 03, 2029Active

Registration details

Analysis ID: c78271a99113c955ecad448bd9b0998a
Customs Code: DHA09402346505

Company information

Manufacturer: DIADENT GROUP INTERNATIONAL
Manufacturer Country: Korea, Republic of
Authorized Representative: TUNG SHENG INTERNATIONAL INC.

Product details

Intended Use: It is limited to the first-level identification scope of the "Root Canal Paper Needle (F.3830)" of the Measures for the Classification and Grading of Medical Devices.
Product Type (Level 1): F Dentistry
Product Type (Level 2): F.3830 Root Canal
Import Information: QMS/QSD;; 輸入

Dates and status

Registration Date: May 03, 2024
Expiry Date: May 03, 2029

About this record

Access comprehensive regulatory information for "Delden" Root Tube Paper Needle (Sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number c78271a99113c955ecad448bd9b0998a and manufactured by DIADENT GROUP INTERNATIONAL. The authorized representative in Taiwan is TUNG SHENG INTERNATIONAL INC..

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