Taiwan FDA registration e34984b41864362cb101ce38c3e67eee

“Denafit” Vacu-Mixer (Non-Sterile)

TW: “帝諾飛特” 維刻矽印模材自動混合機(未滅菌)

Taiwan·Risk Class 1·MD·SHINEO TECHNOLOGY CO., LTD.·Registered Mar 03, 2021 – Mar 03, 2026Expired

Registration details

Analysis ID: e34984b41864362cb101ce38c3e67eee
License Form: Ministry of Health Medical Device Manufacturing No. 008917

Company information

Manufacturer: SHINEO TECHNOLOGY CO., LTD.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: SHINEO TECHNOLOGY CO., LTD.

Product details

Intended Use: Limited to the first level identification range of dental and mercury instruments (F.3100) in the management of medical devices.
Product Type (Level 1): F Dental devices
Product Type (Level 2): F3100 Dental and mercury ware
Import Information: Produced in Taiwan, China

Dates and status

Registration Date: Mar 03, 2021
Expiry Date: Mar 03, 2026

About this record

Access comprehensive regulatory information for “Denafit” Vacu-Mixer (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 e34984b41864362cb101ce38c3e67eee and manufactured by SHINEO TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is SHINEO TECHNOLOGY CO., LTD..

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