Taiwan FDA registration 80a7d92a896e98fd6956775081ea8099
Platinum strontium femur proximal intramedullary nail system
TW: 鉑賽鍶股骨近端髓內釘系統
Taiwan·Risk Class 2·HUANG LIANG BIOMEDICAL TECHNOLOGY CO., LTD.·Registered Dec 12, 2021 – Dec 12, 2026ActiveRegistration details
- Analysis ID
- 80a7d92a896e98fd6956775081ea8099
Company information
- Manufacturer
- HUANG LIANG BIOMEDICAL TECHNOLOGY CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Eric Medical Devices Co., Ltd
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- N Orthopedics
- Product Type (Level 2)
- N.3020 骨髓內固定桿
- Import Information
- Contract manufacturing;; Domestic
Dates and status
- Registration Date
- Dec 12, 2021
- Expiry Date
- Dec 12, 2026
About this record
Access comprehensive regulatory information for Platinum strontium femur proximal intramedullary nail system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 80a7d92a896e98fd6956775081ea8099 and manufactured by HUANG LIANG BIOMEDICAL TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is Eric Medical Devices Co., Ltd.
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