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AQUALAB Urinalysis Tester PU-4010 (Unsterilized) - Taiwan Registration 39160a71b349b94e5bbc74620dd5550c

Access comprehensive regulatory information for AQUALAB Urinalysis Tester PU-4010 (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 39160a71b349b94e5bbc74620dd5550c 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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39160a71b349b94e5bbc74620dd5550c
Registration Details
Taiwan FDA Registration: 39160a71b349b94e5bbc74620dd5550c
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Device Details

AQUALAB Urinalysis Tester PU-4010 (Unsterilized)
TW: โ€œๆ„›็ง‘ไพ†โ€ๅฐฟๆถฒๅˆ†ๆžๆชขๆธฌๅ„€ PU-4010(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

39160a71b349b94e5bbc74620dd5550c

DHA04400877106

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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