Taiwan FDA registration ad09ad46218ecf953eba431bfb9f5263
"Huangliang Biodoctor" mesh fixing system
TW: “皇亮生醫”網片固定系統
Taiwan·Risk Class 2·HUANG LIANG BIOMEDICAL TECHNOLOGY CO., LTD.·Registered Nov 08, 2017 – Nov 08, 2027ActiveRegistration details
- Analysis ID
- ad09ad46218ecf953eba431bfb9f5263
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 Dentistry
- Product Type (Level 2)
- F.4760 骨板;; F.4880 骨內固定螺釘或金屬線
- Import Information
- Domestic
Dates and status
- Registration Date
- Nov 08, 2017
- Expiry Date
- Nov 08, 2027
About this record
Access comprehensive regulatory information for "Huangliang Biodoctor" mesh fixing system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ad09ad46218ecf953eba431bfb9f5263 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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