"DSmedi" Plinth (Non-Sterile)
Taiwan·Risk Class 1·MD·DSMEDI, INC.·Registered Feb 25, 2021 – Feb 25, 2026Cancelled- Analysis ID
- d3f8aab791ee214457d46bf5e9c27afb
- License Form
- Ministry of Health Medical Device Import No. 022340
- Customs Code
- DHA09402234006
- Manufacturer
- DSMEDI, INC.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- HABITZ MEDTECH CO., LTD.
- Product Type (Level 1)
- o Equipment for physical medicine
- Product Type (Level 2)
- O3520 treatment unit
- Import Information
- Imported from abroad
- Registration Date
- Feb 25, 2021
- Expiry Date
- Feb 25, 2026
- Status
- Logged out
- Reason
- 轉為登錄字號
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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.