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Artron Human Chorionic Gonadotropin (HCG) Test System - Taiwan Registration 3bd4dc58dbfb4fcdfc67adec3933959f

Access comprehensive regulatory information for Artron Human Chorionic Gonadotropin (HCG) Test System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3bd4dc58dbfb4fcdfc67adec3933959f and manufactured by ARTRON LABORATORIES INC.. The authorized representative in Taiwan is GORED ENTERPRISE 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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3bd4dc58dbfb4fcdfc67adec3933959f
Registration Details
Taiwan FDA Registration: 3bd4dc58dbfb4fcdfc67adec3933959f
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Device Details

Artron Human Chorionic Gonadotropin (HCG) Test System
TW: ้›…ๅ‰ต้ฉ—ๅญ•ๆธฌ่ฉฆ็ณปๅˆ—
Risk Class 2
MD

Registration Details

3bd4dc58dbfb4fcdfc67adec3933959f

Ministry of Health Medical Device Import No. 031454

DHA05603145402

Company Information

Canada

Product Details

Human chorionic gonadotropin (HCG) in urine was tested by immunoqualitative analysis and preliminarily screened for pregnancy. Available for professional and non-professional use.

A Clinical chemistry and clinical toxicology

A1155 Human chorionic gonadotropin test system

Imported from abroad

Dates and Status

Sep 05, 2018

Sep 05, 2023