Taiwan FDA registration dfe706cee0df2e157f27aa49d7e8b737
“BesTISS” Dental Implant
TW: “皇亮生醫”人工牙根
Taiwan·Risk Class 3·MD·HUANG LIANG BIOMEDICAL TECHNOLOGY CO., LTD.·Registered Nov 11, 2016 – Nov 11, 2026ActiveRegistration details
- Analysis ID
- dfe706cee0df2e157f27aa49d7e8b737
- License Form
- Ministry of Health Medical Device Manufacturing No. 005472
Company information
- Manufacturer
- HUANG LIANG BIOMEDICAL TECHNOLOGY CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- HUANG LIANG BIOMEDICAL TECHNOLOGY CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- F Dental devices
- Product Type (Level 2)
- F3640 Bone explants
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Nov 11, 2016
- Expiry Date
- Nov 11, 2026
About this record
Access comprehensive regulatory information for “BesTISS” Dental Implant in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number dfe706cee0df2e157f27aa49d7e8b737 and manufactured by HUANG LIANG BIOMEDICAL TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is HUANG LIANG BIOMEDICAL TECHNOLOGY CO., LTD..
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