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“D&M” Limb Orthosis(Non-Sterile) - Taiwan Registration 29f73a78eb9e1eaaf7cdf0f888378eab

Access comprehensive regulatory information for “D&M” 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 29f73a78eb9e1eaaf7cdf0f888378eab and manufactured by D&M CO., LTD.. The authorized representative in Taiwan is TAI LUNG CAPITAL INC..

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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29f73a78eb9e1eaaf7cdf0f888378eab
Registration Details
Taiwan FDA Registration: 29f73a78eb9e1eaaf7cdf0f888378eab
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Device Details

“D&M” Limb Orthosis(Non-Sterile)
TW: “迪安姆”肢體護具(未滅菌)
Risk Class 1
MD

Registration Details

29f73a78eb9e1eaaf7cdf0f888378eab

Ministry of Health Medical Device Import Registration No. 006718

DHA08400671802

Company Information

Japan

Product Details

Limited to the first level recognition range of limb equipment (O.3475) of the Measures for the Administration of Medical Devices.

o Equipment for physical medicine

O3475 Body Equipment

Imported from abroad

Dates and Status

Oct 01, 2021

Oct 31, 2023