"Dulac" blood bank centrifuge for in vitro diagnostics (unsterilized)
Taiwan·Risk Class 1·PRINTER DIAGNOSTICS·Registered Nov 06, 2018 – Nov 06, 2023Cancelled- Analysis ID
- 608df277f4b24941b5415502f51ade0b
- Customs Code
- DHA09401978508
- Manufacturer
- PRINTER DIAGNOSTICS
- Manufacturer Country
- United States
- Authorized Representative
- SYNERGY BIOMEDICAL 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
- Nov 06, 2018
- Expiry Date
- Nov 06, 2023
- Cancellation Date
- Sep 30, 2021
- Status
- Logged out
- Reason
- 轉為登錄字號
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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 608df277f4b24941b5415502f51ade0b 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.