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"Horiba" erythrolytic agent (unsterilized) - Taiwan Registration 84d19f6d0ad161a875c1083c54f84719

Access comprehensive regulatory information for "Horiba" erythrolytic agent (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 84d19f6d0ad161a875c1083c54f84719 and manufactured by HORIBA ABX SAS. The authorized representative in Taiwan is HORIBA TAIWAN, INC..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including HORIBA ABX SAS, and 3 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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84d19f6d0ad161a875c1083c54f84719
Registration Details
Taiwan FDA Registration: 84d19f6d0ad161a875c1083c54f84719
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Device Details

"Horiba" erythrolytic agent (unsterilized)
TW: "ๅ €ๅ ด" ็ด…่ก€็ƒๆบถ่งฃๅŠ‘ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

84d19f6d0ad161a875c1083c54f84719

DHA09402292903

Company Information

France

Product Details

Limited to the classification and grading management measures for medical devices, the first level identification range of "red blood cell lytic agent (B.8540)".

B Hematology, pathology, and genetics

B.8540 ็ด…่ก€็ƒๆบถ่งฃๅŠ‘

QMS/QSD;; ่ผธๅ…ฅ

Dates and Status

Oct 18, 2022

Oct 18, 2027

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