"Songan" blood bank centrifuge for in vitro diagnostics (unsterilized)
Taiwan·Risk Class 1·MOOHAN ENTERPRISE CO., LTD.·Registered Oct 01, 2021 – Oct 31, 2025Expired- Analysis ID
- 80b268521f7302e1a5f1dc963ca0baad
- Customs Code
- DHA08401813507
- Manufacturer
- MOOHAN ENTERPRISE CO., LTD.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- Sung Ann Medical Equipment .LTD
- Intended Use
- Limited to the classification and grading management method of medical equipment, in vitro diagnostic blood bank centrifuge (B.9275) first level identification range.
- Product Type (Level 1)
- B Hematology, pathology, and genetics
- Product Type (Level 2)
- B.9275 Blood bank centrifuge for in vitro diagnostics
- Import Information
- Input;; QMS/QSD
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2025
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Access comprehensive regulatory information for "Songan" blood bank centrifuge for in vitro diagnostics (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 80b268521f7302e1a5f1dc963ca0baad and manufactured by MOOHAN ENTERPRISE CO., LTD.. The authorized representative in Taiwan is Sung Ann Medical Equipment .LTD.
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including MOOHAN 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.