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"Renewal" plaque display agent (unsterilized) - Taiwan Registration cf4094dbbe4bc357b9bfdb57ee0299a7

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..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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cf4094dbbe4bc357b9bfdb57ee0299a7
Registration Details
Taiwan FDA Registration: cf4094dbbe4bc357b9bfdb57ee0299a7
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Device Details

"Renewal" plaque display agent (unsterilized)
TW: โ€œ็ถญๆ–ฐโ€ ็‰™่Œๆ–‘้กฏ็คบๅŠ‘ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

cf4094dbbe4bc357b9bfdb57ee0299a7

Company Information

Product Details

Limited to the classification and grading management of medical equipment, the first level identification range of dental hand instruments (F.4565).

F Dentistry

F.4565 ็‰™็ง‘ๆ‰‹็”จๅ™จๆขฐ

Domestic;; Contract manufacturing

Dates and Status

Aug 02, 2021

Aug 02, 2026

Feb 02, 2024