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Jen-Der Medical Insole(Non-Sterile) - Taiwan Registration 0b302925a2a81386b45d88790e09a156

Access comprehensive regulatory information for Jen-Der Medical Insole(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 0b302925a2a81386b45d88790e09a156 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.

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0b302925a2a81386b45d88790e09a156
Registration Details
Taiwan FDA Registration: 0b302925a2a81386b45d88790e09a156
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Device Details

Jen-Der Medical Insole(Non-Sterile)
TW: 正德醫用鞋墊(未滅菌)
Risk Class 1
MD

Registration Details

0b302925a2a81386b45d88790e09a156

Ministry of Health Medical Device Manufacturing Registration No. 000335

DHY08300033504

Company Information

Taiwan, Province of China

Product Details

Auxiliary use with corrective shoes.

o Equipment for physical medicine

O3475 Body Equipment

Produced in Taiwan, China

Dates and Status

Oct 01, 2021

Oct 31, 2025