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"ARKRA" urinalysis tester (unsterilized) - Taiwan Registration be17802aba2a879884a164d04d7044bf

Access comprehensive regulatory information for "ARKRA" urinalysis tester (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number be17802aba2a879884a164d04d7044bf and manufactured by ARKRAY INDUSTRY, INC.. The authorized representative in Taiwan is SYNGEN BIOTECH CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including Arkray Factory Inc., Head office factory, ARKRAY INDUSTRY, INC., and 2 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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be17802aba2a879884a164d04d7044bf
Registration Details
Taiwan FDA Registration: be17802aba2a879884a164d04d7044bf
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Device Details

"ARKRA" urinalysis tester (unsterilized)
TW: "ๆ„›็ง‘ไพ†" ๅฐฟๆถฒๅˆ†ๆžๆชขๆธฌๅ„€ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

be17802aba2a879884a164d04d7044bf

DHA09401605100

Company Information

Philippines

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

QMS/QSD;; ่ผธๅ…ฅ

Dates and Status

Jan 06, 2016

Jan 06, 2026

Sep 30, 2021

Cancellation Information

Logged out

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