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"Horiba" erythrolytic agent (unsterilized) - Taiwan Registration a4b02c64d04bd21d1c1c85ddc85f0020

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 a4b02c64d04bd21d1c1c85ddc85f0020 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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a4b02c64d04bd21d1c1c85ddc85f0020
Registration Details
Taiwan FDA Registration: a4b02c64d04bd21d1c1c85ddc85f0020
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Device Details

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

Registration Details

a4b02c64d04bd21d1c1c85ddc85f0020

DHA09402301704

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‘

Input;; QMS/QSD

Dates and Status

Jan 18, 2023

Jan 18, 2028

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