Taiwan FDA registration 2021897b5eb5fc229b04559f2677e0c2
“Jen-Der” Truncal Orthosis(Non-Sterile)
TW: “正德” 軀幹裝具(未滅菌)
Registration details
- Analysis ID
- 2021897b5eb5fc229b04559f2677e0c2
- License Form
- Ministry of Health Medical Device Manufacturing Registration No. 000453
- Customs Code
- DHY08300045300
Company information
- Manufacturer
- JEN DER P&O APPLIANCES MANUFACTURING CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- JEN DER P&O APPLIANCES MANUFACTURING CO., LTD.
Product details
- Intended Use
- Torso equipment is a medical device used to support or immobilize fractures, injuries with excessive force or sprains to the trunk and neck.
- Product Type (Level 1)
- o Equipment for physical medicine
- Product Type (Level 2)
- O3490 Torso Gear
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2025
About this record
Access comprehensive regulatory information for “Jen-Der” Truncal Orthosis(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 2021897b5eb5fc229b04559f2677e0c2 and manufactured by JEN DER P&O APPLIANCES MANUFACTURING CO., LTD.. The authorized representative in Taiwan is JEN DER P&O APPLIANCES MANUFACTURING 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