Taiwan FDA registration 3e75ea9fed8510f31e03b007edbbdd75

"Diadent" Gutta Percha (Non-Sterile)

TW: "迪爾登" 馬來膠 (未滅菌)

Taiwan·Risk Class 1·MD·DIADENT GROUP INTERNATIONAL·Registered Apr 11, 2017 – Apr 11, 2022Expired

Registration details

Analysis ID: 3e75ea9fed8510f31e03b007edbbdd75
License Form: Ministry of Health Medical Device Import No. 017697
Customs Code: DHA09401769701

Company information

Manufacturer: DIADENT GROUP INTERNATIONAL
Manufacturer Country: Korea, Republic of
Authorized Representative: WAVE PEP TRADE CO., LTD.

Product details

Intended Use: Limited to the first level identification scope of the Measures for the Administration of Medical Equipment "Malay Rubber (F.3850)".
Product Type (Level 1): F Dental devices
Product Type (Level 2): F3850 Male-Glue
Import Information: Imported from abroad

Dates and status

Registration Date: Apr 11, 2017
Expiry Date: Apr 11, 2022

About this record

Access comprehensive regulatory information for "Diadent" Gutta Percha (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 3e75ea9fed8510f31e03b007edbbdd75 and manufactured by DIADENT GROUP INTERNATIONAL. The authorized representative in Taiwan is WAVE PEP TRADE CO., LTD..

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