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"Jen-Der" Crutch (Non-Sterile) - Taiwan Registration 1bb932810fcf489249b1c71976918f0d

Access comprehensive regulatory information for "Jen-Der" Crutch (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 1bb932810fcf489249b1c71976918f0d 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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1bb932810fcf489249b1c71976918f0d
Registration Details
Taiwan FDA Registration: 1bb932810fcf489249b1c71976918f0d
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Device Details

"Jen-Der" Crutch (Non-Sterile)
TW: "ๆญฃๅพท" ้†ซ็™‚็”จๆŸบๆ– (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

1bb932810fcf489249b1c71976918f0d

Ministry of Health Medical Device Manufacturing Registration No. 006261

Company Information

Taiwan, Province of China

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices "Medical Canes (O.3150)".

o Equipment for physical medicine

O3150 Medical cane

Produced in Taiwan, China

Dates and Status

Oct 01, 2021

Oct 31, 2026