Taiwan FDA registration de733a9acfbd37a46cf7b52e8481ac62
"Reted" fiberglass root column (unsterilized)
TW: "雷泰德" 玻璃纖維牙根柱 (未滅菌)
Registration details
- Analysis ID
- de733a9acfbd37a46cf7b52e8481ac62
- Customs Code
- DHA04401302201
Company information
- Manufacturer
- RTD
- Manufacturer Country
- France
- Authorized Representative
- SHI SEI INTERNATIONAL LIMITED
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "Root Canal Center Column Nail (F3810)".
- Product Type (Level 1)
- F Dentistry
- Product Type (Level 2)
- F.3810 Root canal center post
- Import Information
- import
Dates and status
- Registration Date
- May 16, 2013
- Expiry Date
- May 16, 2028
About this record
Access comprehensive regulatory information for "Reted" fiberglass root column (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number de733a9acfbd37a46cf7b52e8481ac62 and manufactured by RTD. The authorized representative in Taiwan is SHI SEI INTERNATIONAL LIMITED.
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