Taiwan FDA registration cad947b40159a526f3e10eacc5e6f1fb
“Socko” SKY Spinal Kyphoplasty System
TW: “碩果”施鈣球囊椎體成形術系統
Registration details
- Analysis ID
- cad947b40159a526f3e10eacc5e6f1fb
- License Form
- Ministry of Health Medical Device Manufacturing No. 007712
Company information
- Manufacturer
- SOCKO MEDICAL CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- SOCKO MEDICAL CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- N Orthopedics
- Product Type (Level 2)
- N0004 Bone Dilation Molding System
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Dec 08, 2022
- Expiry Date
- Dec 08, 2027
About this record
Access comprehensive regulatory information for “Socko” SKY Spinal Kyphoplasty System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number cad947b40159a526f3e10eacc5e6f1fb and manufactured by SOCKO MEDICAL CO., LTD.. The authorized representative in Taiwan is SOCKO MEDICAL 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