Taiwan FDA registration 4f6e57692f240e397be2e980f4b1f181
Jen-Der External Limb Prosthetic Component（Non-Sterile）
TW: 正德體外肢體義肢用組件(未滅菌）
Taiwan·Risk Class 1·MD·JEN DER P&O APPLIANCES MANUFACTURING CO., LTD.·Registered Oct 01, 2021 – Oct 31, 2025ExpiredRegistration details
- Analysis ID
- 4f6e57692f240e397be2e980f4b1f181
- License Form
- Ministry of Health Medical Device Manufacturing Registration No. 000267
- Customs Code
- DHY08300026700
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
- For medical purposes, combined with other suitable objects to form a complete repair device.
- Product Type (Level 1)
- o Equipment for physical medicine
- Product Type (Level 2)
- O3420 Components for in vitro limb prosthetics
- 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 External Limb Prosthetic Component（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 4f6e57692f240e397be2e980f4b1f181 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..
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