Taiwan FDA registration be81e9c5599f0fde56c1e6cab92d6398
"Full fit" bone needle system
TW: “全合”骨針系統
Registration details
- Analysis ID
- be81e9c5599f0fde56c1e6cab92d6398
- Customs Code
- DHY00500250904
Company information
- Manufacturer
- Quanhe Biomedical Technology Co., Ltd
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- AAXTER 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.3040 Smooth or spiral metal bone fixations
- Import Information
- Domestic
Dates and status
- Registration Date
- Oct 01, 2008
- Expiry Date
- Oct 01, 2028
About this record
Access comprehensive regulatory information for "Full fit" bone needle system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number be81e9c5599f0fde56c1e6cab92d6398 and manufactured by Quanhe Biomedical Technology Co., Ltd. The authorized representative in Taiwan is AAXTER 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