Taiwan FDA registration b5af2adb857ef468358fe38ce1fdf3bc
High-viscosity bone cement system for the "Fente Hai" vertebral body
TW: “汎特海”椎體用高黏度骨水泥系統
Taiwan·Risk Class 2·ZHENPENG BIOTECH CO., LTD.·Registered Feb 02, 2023 – Feb 02, 2028ActiveRegistration details
- Analysis ID
- b5af2adb857ef468358fe38ce1fdf3bc
Company information
- Manufacturer
- ZHENPENG BIOTECH CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- XELITE BIOMED LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- N Orthopedics
- Product Type (Level 2)
- N.3027 PMMA骨水泥
- Import Information
- Domestic;; Contract manufacturing
Dates and status
- Registration Date
- Feb 02, 2023
- Expiry Date
- Feb 02, 2028
About this record
Access comprehensive regulatory information for High-viscosity bone cement system for the "Fente Hai" vertebral body in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b5af2adb857ef468358fe38ce1fdf3bc and manufactured by ZHENPENG BIOTECH CO., LTD.. The authorized representative in Taiwan is XELITE BIOMED 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