Taiwan FDA registration a0b8f14cd83215b9948bbd631034ffa9
“TELLUS” Implant-Abutment System
TW: "鈦樂" 支台體系統
Taiwan·Risk Class 2·MD·HUANG LIANG BIOMEDICAL TECHNOLOGY CO., LTD.·Registered Dec 24, 2015 – May 01, 2025ExpiredRegistration details
- Analysis ID
- a0b8f14cd83215b9948bbd631034ffa9
- License Form
- Ministry of Health Medical Device Manufacturing No. 005251
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)
- F3630 Dental bridges for bone explants
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Dec 24, 2015
- Expiry Date
- May 01, 2025
About this record
Access comprehensive regulatory information for “TELLUS” Implant-Abutment System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a0b8f14cd83215b9948bbd631034ffa9 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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