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Beckman Coulter isotonic dilution (non-sterilized) - Taiwan Registration d7995e75e3ebf4bd1b408f130297dfaa

Access comprehensive regulatory information for Beckman Coulter isotonic dilution (non-sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d7995e75e3ebf4bd1b408f130297dfaa and manufactured by BECKMAN COULTER GmbH. The authorized representative in Taiwan is BECKMAN COULTER TAIWAN INC., TAIWAN BRANCH (U.S.A.).

This page provides complete technical specifications, regulatory compliance details. 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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d7995e75e3ebf4bd1b408f130297dfaa
Registration Details
Taiwan FDA Registration: d7995e75e3ebf4bd1b408f130297dfaa
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Device Details

Beckman Coulter isotonic dilution (non-sterilized)
TW: ่ฒๅ…‹ๆ›ผๅบซ็ˆพ็‰น่ก€็ƒ็ญ‰ๅผต็จ€้‡‹ๆถฒ(ๆœชๆป…่Œ)
Risk Class 1

Registration Details

d7995e75e3ebf4bd1b408f130297dfaa

DHA09402345005

Company Information

Product Details

Limited to the first level identification range of "blood cell thinners (B.8200)" of the Measures for the Classification and Grading of Medical Devices.

B Hematology, pathology, and genetics

B.8200 Hemocytodilant

Input;; QMS/QSD

Dates and Status

Apr 19, 2024

Apr 19, 2029