Taiwan FDA registration 51b32c6d650926a3883942346ff4563a
"SHI SEI" Fiber Post (Non-Sterile)
TW: "資生" 玻璃纖維牙根柱 (未滅菌)
Taiwan·Risk Class 1·MD·E. HAHNENKRATT GMBH·Registered Dec 05, 2014 – Dec 05, 2024ExpiredRegistration details
- Analysis ID
- 51b32c6d650926a3883942346ff4563a
- License Form
- Ministry of Health Medical Device Import No. 014723
- Customs Code
- DHA09401472300
Company information
- Manufacturer
- E. HAHNENKRATT GMBH
- Manufacturer Country
- Germany
- 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 (F.3810)".
- Product Type (Level 1)
- F Dental devices
- Product Type (Level 2)
- F3810 tube center column nail
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 05, 2014
- Expiry Date
- Dec 05, 2024
About this record
Access comprehensive regulatory information for "SHI SEI" Fiber Post (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 51b32c6d650926a3883942346ff4563a and manufactured by E. HAHNENKRATT GMBH. The authorized representative in Taiwan is SHI SEI INTERNATIONAL LIMITED.
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