Taiwan FDA registration fbd70e820f2d492d249aaf9979ab8145
“TISS” Implant-Abutment System
TW: “皇亮生醫”支台體系統
Registration details
- Analysis ID
- fbd70e820f2d492d249aaf9979ab8145
- License Form
- Ministry of Health Medical Device Manufacturing No. 004860
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
- May 01, 2015
- Expiry Date
- May 01, 2025
About this record
Access comprehensive regulatory information for “TISS” 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 fbd70e820f2d492d249aaf9979ab8145 and manufactured by HUANG LIANG BIOMEDICAL TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is HUANG LIANG BIOMEDICAL TECHNOLOGY CO., LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices