Taiwan FDA registration fe8b88f699b1a5f9565ec327e74fffcf
“BONART” Curing Light Unit and Accessories
TW: “慶暐”光固化機及其附件
Registration details
- Analysis ID
- fe8b88f699b1a5f9565ec327e74fffcf
- License Form
- Ministry of Health Medical Device Manufacturing No. 004502
Company information
- Manufacturer
- BONART CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- BONART CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- F Dental devices
- Product Type (Level 2)
- F6070 UV activator for polymerization
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Mar 28, 2014
- Expiry Date
- Mar 28, 2024
About this record
Access comprehensive regulatory information for “BONART” Curing Light Unit and Accessories in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fe8b88f699b1a5f9565ec327e74fffcf and manufactured by BONART CO., LTD.. The authorized representative in Taiwan is BONART 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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