Taiwan FDA registration 548bde2caab822402f5a36b523a5e202
Apex Knee Osteotomy Correction System
TW: 愛派司膝關節截骨矯正系統
Taiwan·Risk Class 2·A PLUS BIOTECHNOLOGY CO., LTD.·Registered Aug 08, 2018 – Aug 08, 2028ActiveRegistration details
- Analysis ID
- 548bde2caab822402f5a36b523a5e202
Company information
- Manufacturer
- A PLUS BIOTECHNOLOGY CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- A PLUS BIOTECHNOLOGY 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
Dates and status
- Registration Date
- Aug 08, 2018
- Expiry Date
- Aug 08, 2028
About this record
Access comprehensive regulatory information for Apex Knee Osteotomy Correction System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 548bde2caab822402f5a36b523a5e202 and manufactured by A PLUS BIOTECHNOLOGY CO., LTD.. The authorized representative in Taiwan is A PLUS BIOTECHNOLOGY 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