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“JEN-DER” LIMB ORTHOSIS(Non-Sterile) - Taiwan Registration 2d24b71b71c110135416b12a0dd5372f

Access comprehensive regulatory information for “JEN-DER” LIMB 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 2d24b71b71c110135416b12a0dd5372f 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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2d24b71b71c110135416b12a0dd5372f
Registration Details
Taiwan FDA Registration: 2d24b71b71c110135416b12a0dd5372f
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Device Details

“JEN-DER” LIMB ORTHOSIS(Non-Sterile)
TW: “正德” 肢體裝具(未滅菌)
Risk Class 1
MD

Registration Details

2d24b71b71c110135416b12a0dd5372f

Ministry of Health Medical Device Manufacturing Registration No. 000160

DHY08300016008

Company Information

Taiwan, Province of China

Product Details

Medical equipment worn on the upper or lower limbs to support, correct, prevent deformation or straighten the body structure for functional improvement.

o Equipment for physical medicine

O3475 Body Equipment

Produced in Taiwan, China

Dates and Status

Oct 01, 2021

Oct 31, 2025