Taiwan FDA registration aa13549d9ac12670bd0c89db19a3e393
"Bassi" Gutta Percha Points (Non-Sterile)
TW: 巴斯馬來膠針 (未滅菌)
Taiwan·Risk Class 1·MD·SURE DENT CORPORATION·Registered Nov 20, 2019 – Nov 20, 2024ExpiredRegistration details
- Analysis ID
- aa13549d9ac12670bd0c89db19a3e393
- License Form
- Ministry of Health Medical Device Import No. 021028
- Customs Code
- DHA09402102802
Company information
- Manufacturer
- SURE DENT CORPORATION
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- UNIGLIFE BIOMED CO., 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
- Nov 20, 2019
- Expiry Date
- Nov 20, 2024
About this record
Access comprehensive regulatory information for "Bassi" 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 aa13549d9ac12670bd0c89db19a3e393 and manufactured by SURE DENT CORPORATION. The authorized representative in Taiwan is UNIGLIFE BIOMED CO., LTD..
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