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"Arn" blood bank centrifuge for in vitro diagnostics (unsterilized) - Taiwan Registration 5c856f549ff56c51dededc0718f3553c

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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5c856f549ff56c51dededc0718f3553c
Registration Details
Taiwan FDA Registration: 5c856f549ff56c51dededc0718f3553c
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Device Details

"Arn" blood bank centrifuge for in vitro diagnostics (unsterilized)
TW: "ไบžๆฉ" ้ซ”ๅค–่จบๆ–ท็”จ่ก€ๅบซ้›ขๅฟƒๆฉŸ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

5c856f549ff56c51dededc0718f3553c

DHA086a0011300

Company Information

Product Details

Limited to the classification and grading management method of medical equipment, in vitro diagnostic blood bank centrifuge (B.9275) first level identification range.

B Hematology, pathology, and genetics

B.9275 Blood bank centrifuge for in vitro diagnostics

Dates and Status

May 15, 2023

Oct 31, 2025