Taiwan FDA registration db03d8f50bc1caff8672873647e32516
“TISS” GBR-Tent Screw
TW: “皇亮生醫”牙科補骨支撐螺釘
Taiwan·Risk Class 2·MD·HUANG LIANG BIOMEDICAL TECHNOLOGY CO., LTD.·Registered Jul 04, 2017 – Jul 04, 2027ActiveRegistration details
- Analysis ID
- db03d8f50bc1caff8672873647e32516
- License Form
- Ministry of Health Medical Device Manufacturing No. 005882
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)
- F4880 Intraosseous fixing screws or metal wires
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Jul 04, 2017
- Expiry Date
- Jul 04, 2027
About this record
Access comprehensive regulatory information for “TISS” GBR-Tent Screw in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number db03d8f50bc1caff8672873647e32516 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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