Taiwan FDA registration fed0703c06fb1e38d4227fc7f24b0bb8
“jRafa” Bone Filler Delivery System (Non-sterile)
TW: “拉伐”骨填充物注射系統(未滅菌)
Registration details
- Analysis ID
- fed0703c06fb1e38d4227fc7f24b0bb8
- License Form
- Ministry of Health Medical Device Manufacturing No. 007672
Company information
- Manufacturer
- JOY MEDICAL DEVICES CORPORATION
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- JOY MEDICAL DEVICES CORPORATION
Product details
- Intended Use
- Limited to the first level identification range of the bone cement dispenser (N.4200) of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- N Orthopedic devices
- Product Type (Level 2)
- N4200 Bone cement dispenser
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Mar 08, 2019
- Expiry Date
- Mar 08, 2024
About this record
Access comprehensive regulatory information for “jRafa” Bone Filler Delivery System (Non-sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number fed0703c06fb1e38d4227fc7f24b0bb8 and manufactured by JOY MEDICAL DEVICES CORPORATION. The authorized representative in Taiwan is JOY MEDICAL DEVICES CORPORATION.
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