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"Miyasu Kimori" Fully automatic urine and fluid analyzer (unsterilized) - Taiwan Registration 8586f54d3dbec2a4ad71d012a3406d6e

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 8586f54d3dbec2a4ad71d012a3406d6e and manufactured by 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;; 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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8586f54d3dbec2a4ad71d012a3406d6e
Registration Details
Taiwan FDA Registration: 8586f54d3dbec2a4ad71d012a3406d6e
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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
Cancelled

Registration Details

8586f54d3dbec2a4ad71d012a3406d6e

DHA09401631100

Company Information

Product Details

Limited to the first level identification range of the "Automatic Urinalysis System (A.2900)" of the Measures for the Administration of Medical Devices.

A Clinical chemistry and clinical toxicology

A.2900 Automated urinalysis system

Input;; QMS/QSD

Dates and Status

Mar 23, 2016

Mar 23, 2026

Sep 30, 2021

Cancellation Information

Logged out

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