"Songan" blood bank centrifuge for in vitro diagnostics (unsterilized)
Taiwan·Risk Class 1·MOOHAN ENTERPRISE CO., LTD.·Registered Aug 01, 2017 – Aug 01, 2022Cancelled- Analysis ID
- 1c5c7557564b43b66893d276344ea9d5
- Customs Code
- DHA09401813503
- Manufacturer
- MOOHAN ENTERPRISE CO., LTD.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- Sung Ann Medical Equipment .LTD
- Intended Use
- Limited to the first level identification range of blood bank centrifuge (B.9275) for in vitro diagnostic of medical equipment management methods.
- Product Type (Level 1)
- B Hematology, pathology, and genetics
- Product Type (Level 2)
- B.9275 Blood bank centrifuge for in vitro diagnostics
- Import Information
- QMS/QSD;; 輸入
- Registration Date
- Aug 01, 2017
- Expiry Date
- Aug 01, 2022
- Cancellation Date
- Sep 30, 2021
- Status
- Logged out
- Reason
- 轉為登錄字號
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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 1c5c7557564b43b66893d276344ea9d5 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.