"DSmedi" Plinth (Non-Sterile)
Taiwan·Risk Class 1·MD·DSMEDI, INC.·Registered Oct 01, 2021 – Oct 31, 2026Active- Analysis ID
- 55d034bae9a09db72c44308e6ea71033
- License Form
- Ministry of Health Medical Device Import Registration No. 022340
- Customs Code
- DHA08402234000
- Manufacturer
- DSMEDI, INC.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- HABITZ MEDTECH CO., LTD.
- Intended Use
- Limited to the first-level identification range of the Measures for the Administration of Medical Equipment "Treatment Table (O.3520)".
- Product Type (Level 1)
- o Equipment for physical medicine
- Product Type (Level 2)
- O3520 treatment unit
- Import Information
- Imported from abroad
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2026
Top companies providing products similar to ""DSmedi" Plinth (Non-Sterile)"
Recently registered similar products
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 55d034bae9a09db72c44308e6ea71033 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.