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"Miyasu Kimori" Fully automatic urine and fluid analyzer (unsterilized) - Taiwan Registration e464026be8f53e5a57066f701d628c79

Access comprehensive regulatory information for "Miyasu Kimori" Fully automatic urine and fluid analyzer (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e464026be8f53e5a57066f701d628c79 and manufactured by SYSMEX CORPORATION;; SYSMEX CORPORATION, I-SQUARE. The authorized representative in Taiwan is SYSMEX TAIWAN CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including SYSMEX CORPORATION, I-SQUARE, 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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e464026be8f53e5a57066f701d628c79
Registration Details
Taiwan FDA Registration: e464026be8f53e5a57066f701d628c79
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Device Details

"Miyasu Kimori" Fully automatic urine and fluid analyzer (unsterilized)
TW: "ๅธŒๆฃฎ็พŽๅบท" ๅ…จ่‡ชๅ‹•ๅฐฟๆถฒๅˆ†ๆžๅ„€ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

e464026be8f53e5a57066f701d628c79

DHA08401631104

Company Information

Product Details

Limited to the first level identification range of the "Automated Urinalysis System (A.2900)" of the Measures for the Classification and Grading of Medical Devices.

A Clinical chemistry and clinical toxicology

A.2900 Automated urinalysis system

Input;; QMS/QSD

Dates and Status

Oct 01, 2021

Oct 31, 2026

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