Taiwan FDA registration a0447f59634f15c342fb9fa7c3a95426
"Frankfurt" corrective line (unsterilized)
TW: "法蘭克福" 矯正線 (未滅菌)
Registration details
- Analysis ID
- a0447f59634f15c342fb9fa7c3a95426
- Customs Code
- DHA09600269304
Company information
- Manufacturer
- SHENZHEN SUPERLINE TECHNOLOGY CO., LTD.
- Manufacturer Country
- China
- Authorized Representative
- FRANKFURT TECHNOLOGY CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of medical equipment classification and grading management measures, dental orthodontic devices and their accessories (F.5410).
- Product Type (Level 1)
- F Dentistry
- Product Type (Level 2)
- F.5410 Dental orthodox equipment and accessories thereof
- Import Information
- Input;; Chinese goods
Dates and status
- Registration Date
- Apr 15, 2016
- Expiry Date
- Apr 15, 2026
About this record
Access comprehensive regulatory information for "Frankfurt" corrective line (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a0447f59634f15c342fb9fa7c3a95426 and manufactured by SHENZHEN SUPERLINE TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is FRANKFURT TECHNOLOGY CO., LTD..
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