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"DSmedi" Plinth (Non-Sterile) - Taiwan Registration d3f8aab791ee214457d46bf5e9c27afb

Access comprehensive regulatory information for "DSmedi" Plinth (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 d3f8aab791ee214457d46bf5e9c27afb and manufactured by DSMEDI, INC.. The authorized representative in Taiwan is HABITZ MEDTECH CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including DSMEDI, INC., and 1 recent registrations in the same category. 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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d3f8aab791ee214457d46bf5e9c27afb
Registration Details
Taiwan FDA Registration: d3f8aab791ee214457d46bf5e9c27afb
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Device Details

"DSmedi" Plinth (Non-Sterile)
TW: "่ฟชๆ–ฏๆข…่ฟช" ๆฒป็™‚ๆชฏ(ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

d3f8aab791ee214457d46bf5e9c27afb

Ministry of Health Medical Device Import No. 022340

DHA09402234006

Company Information

Korea, Republic of

Product Details

o Equipment for physical medicine

O3520 treatment unit

Imported from abroad

Dates and Status

Feb 25, 2021

Feb 25, 2026

Cancellation Information

Logged out

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