Taiwan FDA registration d7296227df4468bccba7c3d02aa13151
“TELLUS” Anchorage Screws
TW: “鈦樂”牙科矯正釘
Taiwan·Risk Class 3·MD·HUANG LIANG BIOMEDICAL TECHNOLOGY CO., LTD.·Registered Dec 05, 2017 – Mar 23, 2027ActiveRegistration details
- Analysis ID
- d7296227df4468bccba7c3d02aa13151
- License Form
- Ministry of Health Medical Device Manufacturing No. 006009
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
- Dec 05, 2017
- Expiry Date
- Mar 23, 2027
About this record
Access comprehensive regulatory information for “TELLUS” Anchorage Screws in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number d7296227df4468bccba7c3d02aa13151 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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