Taiwan FDA registration 21e8a7c11d13986b8614dc4047d6498d
“WELL-DAY” Continuous Passive Motion Device (Non-Sterile)
TW: “晶晏” 連續式被動關節活動器 (未滅菌)
Taiwan·Risk Class 1·MD·Jingyan International Enterprise Co., Ltd. Kamioka Factory·Registered May 05, 2023 – May 05, 2028ActiveRegistration details
- Analysis ID
- 21e8a7c11d13986b8614dc4047d6498d
- License Form
- Ministry of Health Medical Device Manufacturing No. 009866
Company information
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- WELL-DAY INTERNATIONAL LTD.
Product details
- Intended Use
- Limited to the first level identification range of the classification and grading management method for medical equipment "Continuous Passive Joint Activator (O.0006)".
- Product Type (Level 1)
- o Physical Medical Sciences
- Product Type (Level 2)
- O0006 Continuous Passive Joint Activator
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- May 05, 2023
- Expiry Date
- May 05, 2028
About this record
Access comprehensive regulatory information for “WELL-DAY” Continuous Passive Motion Device (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 21e8a7c11d13986b8614dc4047d6498d and manufactured by Jingyan International Enterprise Co., Ltd. Kamioka Factory. The authorized representative in Taiwan is WELL-DAY INTERNATIONAL 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