Taiwan FDA registration 836d2b9be3e3db400ae9fad25c752889
"DIADENT" Gutta Percha Points (Non-Sterile)
TW: "黛爾登" 馬來膠針(未滅菌)
Taiwan·Risk Class 1·MD·DIADENT GROUP INTERNATIONAL (KOREA & INTERNATIONAL)·Registered Apr 30, 2015 – Apr 30, 2025ExpiredRegistration details
- Analysis ID
- 836d2b9be3e3db400ae9fad25c752889
- License Form
- Ministry of Health Medical Device Import No. 015184
- Customs Code
- DHA09401518401
Company information
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- SHI SEI INTERNATIONAL LIMITED
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Equipment "Malay Rubber (F.3850)".
- Product Type (Level 1)
- F Dental devices
- Product Type (Level 2)
- F3850 Male-Glue
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Apr 30, 2015
- Expiry Date
- Apr 30, 2025
About this record
Access comprehensive regulatory information for "DIADENT" Gutta Percha Points (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 836d2b9be3e3db400ae9fad25c752889 and manufactured by DIADENT GROUP INTERNATIONAL (KOREA & INTERNATIONAL). The authorized representative in Taiwan is SHI SEI INTERNATIONAL LIMITED.
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