Taiwan FDA registration d6b1be7e3ff25fcc8270223e64f420a6
"Aocheng" dissolving type locking compression bone plate system
TW: “奧澄”解部型鎖定加壓骨板系統
Taiwan·Risk Class 2·HUANG LIANG BIOMEDICAL TECHNOLOGY CO., LTD.·Registered Feb 17, 2022 – Feb 17, 2027ActiveRegistration details
- Analysis ID
- d6b1be7e3ff25fcc8270223e64f420a6
Company information
- Manufacturer
- HUANG LIANG BIOMEDICAL TECHNOLOGY CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Ocean Biomedical 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.3030 Single or multiple metallic bone fixation devices and accessories
- Import Information
- Domestic;; Contract manufacturing
Dates and status
- Registration Date
- Feb 17, 2022
- Expiry Date
- Feb 17, 2027
About this record
Access comprehensive regulatory information for "Aocheng" dissolving type locking compression bone plate system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d6b1be7e3ff25fcc8270223e64f420a6 and manufactured by HUANG LIANG BIOMEDICAL TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is Ocean Biomedical Co., Ltd..
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