Taiwan FDA registration 81642e4a4d4e97b287f12cf3813000c4
"Ocheng" anatomical radius locking compression bone plate system
TW: “奧澄”解剖型橈骨鎖定加壓骨板系統
Taiwan·Risk Class 2·HUANG LIANG BIOMEDICAL TECHNOLOGY CO., LTD.·Registered Jan 02, 2021 – Jan 02, 2026ExpiredRegistration details
- Analysis ID
- 81642e4a4d4e97b287f12cf3813000c4
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
- For details, it is Chinese approved copy of the imitation order
- 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
- Jan 02, 2021
- Expiry Date
- Jan 02, 2026
About this record
Access comprehensive regulatory information for "Ocheng" anatomical radius 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 81642e4a4d4e97b287f12cf3813000c4 and manufactured by HUANG LIANG BIOMEDICAL TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is Ocean Biomedical 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