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Jen-Der External Limb Prosthetic Component(Non-Sterile) - Taiwan Registration 4f6e57692f240e397be2e980f4b1f181

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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4f6e57692f240e397be2e980f4b1f181
Registration Details
Taiwan FDA Registration: 4f6e57692f240e397be2e980f4b1f181
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Device Details

Jen-Der External Limb Prosthetic Component(Non-Sterile)
TW: 正德體外肢體義肢用組件(未滅菌)
Risk Class 1
MD

Registration Details

4f6e57692f240e397be2e980f4b1f181

Ministry of Health Medical Device Manufacturing Registration No. 000267

DHY08300026700

Company Information

Taiwan, Province of China

Product Details

For medical purposes, combined with other suitable objects to form a complete repair device.

o Equipment for physical medicine

O3420 Components for in vitro limb prosthetics

Produced in Taiwan, China

Dates and Status

Oct 01, 2021

Oct 31, 2025