"Khanma" warm chamber (unsterilized)
Taiwan·Risk Class 1·SHIAN JIA MEEI ENTERPRISE CO., LTD.·Registered Oct 01, 2021 – Oct 31, 2026Active- Analysis ID
- fa12027813f6d300ca96709abeb6b72c
- Manufacturer
- SHIAN JIA MEEI ENTERPRISE CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- SHIAN JIA MEEI ENTERPRISE CO., LTD.
- Intended Use
- Limited to the first level identification scope of the "Power Hot Compress Mat (O.5740)" of the Measures for the Classification and Grading of Medical Equipment.
- Product Type (Level 1)
- o Physical Medical Sciences
- Product Type (Level 2)
- O.5740 動力式熱敷墊
- Import Information
- 國產;; QMS/QSD
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2026
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Access comprehensive regulatory information for "Khanma" warm chamber (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number fa12027813f6d300ca96709abeb6b72c and manufactured by SHIAN JIA MEEI ENTERPRISE CO., LTD.. The authorized representative in Taiwan is SHIAN JIA MEEI ENTERPRISE CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including SHIAN JIA MEEI ENTERPRISE CO., LTD., 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.