Taiwan FDA registration 4816f22c84356e337511bd0ba3746998
"Shiheng" bone cement mixer (unsterilized)
TW: “世亨”骨水泥攪拌器 (未滅菌)
Taiwan·Risk Class 1·SHI HENG TECHNOLOGY CO., LTD.·Registered Apr 09, 2010 – Apr 09, 2025ExpiredRegistration details
- Analysis ID
- 4816f22c84356e337511bd0ba3746998
Company information
- Manufacturer
- SHI HENG TECHNOLOGY CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- SHI HENG TECHNOLOGY CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the "Clinical Bone Cement Mixer (N.4210)" of the Measures for the Classification and Grading Management of Medical Equipment.
- Product Type (Level 1)
- N Orthopedics
- Product Type (Level 2)
- N.4210 臨床用骨水泥攪拌器
- Import Information
- Domestic
Dates and status
- Registration Date
- Apr 09, 2010
- Expiry Date
- Apr 09, 2025
About this record
Access comprehensive regulatory information for "Shiheng" bone cement mixer (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 4816f22c84356e337511bd0ba3746998 and manufactured by SHI HENG TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is SHI HENG TECHNOLOGY 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