Taiwan FDA registration 7b7db8cd6748941cb8484209dc99e8a2
"Dianfeng" grinding device and its accessories (unsterilized)
TW: “典鋒” 研磨裝置及其附件 (未滅菌)
Taiwan·Risk Class 1·SHENZHEN DIAN FONG ABRASIVES CO., LTD.·Registered Aug 26, 2022 – Oct 31, 2024ExpiredRegistration details
- Analysis ID
- 7b7db8cd6748941cb8484209dc99e8a2
- Customs Code
- DHA086a0006900
Company information
- Manufacturer
- SHENZHEN DIAN FONG ABRASIVES CO., LTD.
- Manufacturer Country
- China
- Authorized Representative
- HUANG YA BIOMEDICAL TECHNOLOGY LTD.
Product details
- Intended Use
- Limited to the first level identification range of grinding devices and their accessories (F.6010) of the classification and grading management methods for medical equipment.
- Product Type (Level 1)
- F Dentistry
- Product Type (Level 2)
- F.6010 Abrasive devices and accessories thereof
Dates and status
- Registration Date
- Aug 26, 2022
- Expiry Date
- Oct 31, 2024
About this record
Access comprehensive regulatory information for "Dianfeng" grinding device and its accessories (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 7b7db8cd6748941cb8484209dc99e8a2 and manufactured by SHENZHEN DIAN FONG ABRASIVES CO., LTD.. The authorized representative in Taiwan is HUANG YA BIOMEDICAL TECHNOLOGY LTD..
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