"Acerys" blood bank centrifuge for in vitro diagnostics (unsterilized)
Taiwan·Risk Class 1·ARTHREX, INC.·Registered Nov 08, 2011 – Nov 08, 2026Cancelled- Analysis ID
- dd390e7aea54455c6387024081cee753
- Customs Code
- DHA04401103500
- Manufacturer
- ARTHREX, INC.
- Manufacturer Country
- United States
- Authorized Representative
- JOINSMART BIOMEDICAL COMPANY LIMITED
- 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 08, 2011
- Expiry Date
- Nov 08, 2026
- Cancellation Date
- Sep 30, 2021
- Status
- Logged out
- Reason
- 轉為登錄字號
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Access comprehensive regulatory information for "Acerys" 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 dd390e7aea54455c6387024081cee753 and manufactured by ARTHREX, INC.. The authorized representative in Taiwan is JOINSMART BIOMEDICAL COMPANY LIMITED.
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including ARTHREX, INC., 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.