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"Diadent" Gutta Percha (Non-Sterile) - Taiwan Registration 3e75ea9fed8510f31e03b007edbbdd75

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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3e75ea9fed8510f31e03b007edbbdd75
Registration Details
Taiwan FDA Registration: 3e75ea9fed8510f31e03b007edbbdd75
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Device Details

"Diadent" Gutta Percha (Non-Sterile)
TW: "่ฟช็ˆพ็™ป" ้ฆฌไพ†่†  (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

3e75ea9fed8510f31e03b007edbbdd75

Ministry of Health Medical Device Import No. 017697

DHA09401769701

Company Information

Korea, Republic of

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Equipment "Malay Rubber (F.3850)".

F Dental devices

F3850 Male-Glue

Imported from abroad

Dates and Status

Apr 11, 2017

Apr 11, 2022