Taiwan FDA registration cf4094dbbe4bc357b9bfdb57ee0299a7

"Renewal" plaque display agent (unsterilized)

TW: “維新” 牙菌斑顯示劑 (未滅菌)

Taiwan·Risk Class 1·Vita Technology Co., Ltd.;; Hanqiang Biotechnology Co., Ltd·Registered Aug 02, 2021 – Aug 02, 2026Active

Registration details

Analysis ID: cf4094dbbe4bc357b9bfdb57ee0299a7

Company information

Manufacturer: Vita Technology Co., Ltd.;; Hanqiang Biotechnology Co., Ltd
Manufacturer Country: Taiwan, Province of China
Authorized Representative: WEI-SHIN BIOTECHNOLOGY CO., LTD.

Product details

Intended Use: Limited to the classification and grading management of medical equipment, the first level identification range of dental hand instruments (F.4565).
Product Type (Level 1): F Dentistry
Product Type (Level 2): F.4565 牙科手用器械
Import Information: Domestic;; Contract manufacturing

Dates and status

Registration Date: Aug 02, 2021
Expiry Date: Aug 02, 2026
Cancellation Date: Feb 02, 2024

About this record

Access comprehensive regulatory information for "Renewal" plaque display agent (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number cf4094dbbe4bc357b9bfdb57ee0299a7 and manufactured by Vita Technology Co., Ltd.;; Hanqiang Biotechnology Co., Ltd. The authorized representative in Taiwan is WEI-SHIN BIOTECHNOLOGY CO., LTD..

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