Taiwan FDA registration b20a1782e6d6de6a02f8ac393e749615
"Osumi" rib fixation system
TW: “奧澄”肋骨固定系統
Registration details
- Analysis ID
- b20a1782e6d6de6a02f8ac393e749615
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
- Contract manufacturing;; Domestic
Dates and status
- Registration Date
- Jan 02, 2021
- Expiry Date
- Jan 02, 2026
About this record
Access comprehensive regulatory information for "Osumi" rib fixation system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b20a1782e6d6de6a02f8ac393e749615 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