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"AGCO" Automatic Urine Analyzer AE-4020 (Unsterilized) - Taiwan Registration df3943a24a7e66857bc39327137e9b23

Access comprehensive regulatory information for "AGCO" Automatic Urine Analyzer AE-4020 (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number df3943a24a7e66857bc39327137e9b23 and manufactured by ARKRAY FACTORY INC.. The authorized representative in Taiwan is MEDTRI CO., LTD..

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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df3943a24a7e66857bc39327137e9b23
Registration Details
Taiwan FDA Registration: df3943a24a7e66857bc39327137e9b23
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Device Details

"AGCO" Automatic Urine Analyzer AE-4020 (Unsterilized)
TW: โ€œๆ„›็ง‘ไพ†โ€่‡ชๅ‹•ๅฐฟๆถฒๅˆ†ๆžๅ„€ AE-4020(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

df3943a24a7e66857bc39327137e9b23

DHA04400877300

Company Information

Japan

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

import

Dates and Status

Apr 26, 2010

Apr 26, 2025

Sep 30, 2021

Cancellation Information

Logged out

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