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"Songan" blood bank centrifuge for in vitro diagnostics (unsterilized) - Taiwan Registration 80b268521f7302e1a5f1dc963ca0baad

Access comprehensive regulatory information for "Songan" 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 80b268521f7302e1a5f1dc963ca0baad and manufactured by MOOHAN ENTERPRISE CO., LTD.. The authorized representative in Taiwan is Sung Ann Medical Equipment .LTD.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including MOOHAN ENTERPRISE CO., LTD., 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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80b268521f7302e1a5f1dc963ca0baad
Registration Details
Taiwan FDA Registration: 80b268521f7302e1a5f1dc963ca0baad
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Device Details

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

Registration Details

80b268521f7302e1a5f1dc963ca0baad

DHA08401813507

Company Information

Korea, Republic of

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

Input;; QMS/QSD

Dates and Status

Oct 01, 2021

Oct 31, 2025

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