Taiwan FDA registration 323406df01d7827ae0bc08eb3f90133e
"SPIDENT" Gutta Percha (Non-Sterile)
TW: "史百登" 馬來膠 (未滅菌)
Taiwan·Risk Class 1·MD·SPIDENT CO., LTD.·Registered Jun 18, 2015 – Jun 18, 2025ExpiredRegistration details
- Analysis ID
- 323406df01d7827ae0bc08eb3f90133e
- License Form
- Ministry of Health Medical Device Import No. 015365
- Customs Code
- DHA09401536505
Company information
- Manufacturer
- SPIDENT CO., LTD.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- THONG TING TRADING COMPANY LTD.
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
- Jun 18, 2015
- Expiry Date
- Jun 18, 2025
About this record
Access comprehensive regulatory information for "SPIDENT" Gutta Percha (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 323406df01d7827ae0bc08eb3f90133e and manufactured by SPIDENT CO., LTD.. The authorized representative in Taiwan is THONG TING TRADING COMPANY LTD..
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