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"Arkra" urine analyzer (unsterilized) - Taiwan Registration 2a4dc6e0ff32abfbcbad557efacbc84e

Access comprehensive regulatory information for "Arkra" urine 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 2a4dc6e0ff32abfbcbad557efacbc84e and manufactured by ARKRAY FACTORY INC.. The authorized representative in Taiwan is SYNGEN BIOTECH 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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2a4dc6e0ff32abfbcbad557efacbc84e
Registration Details
Taiwan FDA Registration: 2a4dc6e0ff32abfbcbad557efacbc84e
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Device Details

"Arkra" urine analyzer (unsterilized)
TW: ใ€ๆ„›็ง‘ไพ†ใ€žๅฐฟๆถฒๅˆ†ๆžๅ„€ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

2a4dc6e0ff32abfbcbad557efacbc84e

DHA04400974102

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

Dec 24, 2010

Dec 24, 2015

Apr 25, 2018

Cancellation Information

Logged out

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