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"Acerys" blood bank centrifuge for in vitro diagnostics (unsterilized) - Taiwan Registration 0421240415952f264bf06d8a8cd2a10f

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 0421240415952f264bf06d8a8cd2a10f 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.

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0421240415952f264bf06d8a8cd2a10f
Registration Details
Taiwan FDA Registration: 0421240415952f264bf06d8a8cd2a10f
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Device Details

"Acerys" blood bank centrifuge for in vitro diagnostics (unsterilized)
TW: "่‰พๆ€็‘žๆ–ฏ" ้ซ”ๅค–่จบๆ–ท็”จ่ก€ๅบซ้›ขๅฟƒๆฉŸ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

0421240415952f264bf06d8a8cd2a10f

DHA08401103507

Company Information

United States

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

QMS/QSD;; ่ผธๅ…ฅ

Dates and Status

Oct 01, 2021

Oct 31, 2027

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