Taiwan FDA registration 52f9acafd86dbdc69dd1e1a95ad4bad9
"Qingwei" light curing machine and its accessories
TW: “慶暐”光固化機及其附件
Taiwan·Risk Class 2·BONART CO., LTD.·Registered Jan 07, 2009 – Jan 07, 2014CancelledRegistration details
- Analysis ID
- 52f9acafd86dbdc69dd1e1a95ad4bad9
- Customs Code
- DHY00500263002
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 Dentistry
- Product Type (Level 2)
- F.6070 Ultraviolet Activator for Polymerization
- Import Information
- Domestic
Dates and status
- Registration Date
- Jan 07, 2009
- Expiry Date
- Jan 07, 2014
- Cancellation Date
- Nov 15, 2016
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Qingwei" light curing machine and its accessories in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 52f9acafd86dbdc69dd1e1a95ad4bad9 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.
Free DatabasePowered by Pure Global AI89,000+ Devices