Taiwan FDA registration 7dc12e705124d9850d3cdeab9c26c211
"Qingwei" bone knife head
TW: “慶暐”骨刀機頭
Taiwan·Risk Class 2·BONART CO., LTD.·Registered Oct 13, 2008 – Oct 13, 2028ActiveRegistration details
- Analysis ID
- 7dc12e705124d9850d3cdeab9c26c211
- Customs Code
- DHY00500253505
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.4120 Bone cutters and accessories thereof
- Import Information
- Domestic
Dates and status
- Registration Date
- Oct 13, 2008
- Expiry Date
- Oct 13, 2028
About this record
Access comprehensive regulatory information for "Qingwei" bone knife head in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7dc12e705124d9850d3cdeab9c26c211 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