Taiwan FDA registration 5c856f549ff56c51dededc0718f3553c
"Arn" blood bank centrifuge for in vitro diagnostics (unsterilized)
TW: "亞恩" 體外診斷用血庫離心機 (未滅菌)
Taiwan·Risk Class 1·HUNAN XIANG YI LABORATORY INSTRUMENT DEVELOPMENT CO., LTD.·Registered May 15, 2023 – Oct 31, 2025ExpiredRegistration details
- Analysis ID
- 5c856f549ff56c51dededc0718f3553c
- Customs Code
- DHA086a0011300
Company information
- Manufacturer Country
- China
- Authorized Representative
- AEON BIOTHERAPEUTICS CORP.
Product details
- 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
Dates and status
- Registration Date
- May 15, 2023
- Expiry Date
- Oct 31, 2025
About this record
Access comprehensive regulatory information for "Arn" 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 5c856f549ff56c51dededc0718f3553c and manufactured by HUNAN XIANG YI LABORATORY INSTRUMENT DEVELOPMENT CO., LTD.. The authorized representative in Taiwan is AEON BIOTHERAPEUTICS CORP..
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