"Dulac" blood bank centrifuge for in vitro diagnostics (unsterilized)
Taiwan·Risk Class 1·PRINTER DIAGNOSTICS·Registered Oct 01, 2021 – Oct 31, 2025Expired- Analysis ID
- 282e713729bc221baa4bd5ac5b4bd225
- Customs Code
- DHA08401978502
- Manufacturer
- PRINTER DIAGNOSTICS
- Manufacturer Country
- United States
- Authorized Representative
- SYNERGY BIOMEDICAL 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
- QMS/QSD;; 輸入
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2025
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Access comprehensive regulatory information for "Dulac" 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 282e713729bc221baa4bd5ac5b4bd225 and manufactured by PRINTER DIAGNOSTICS. The authorized representative in Taiwan is SYNERGY BIOMEDICAL LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including PRINTER DIAGNOSTICS, 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.