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"Artron" MICROALBUMIN TEST(Non-Sterile) - Taiwan Registration e7758b533692596f140d527197173355

Access comprehensive regulatory information for "Artron" MICROALBUMIN TEST(Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e7758b533692596f140d527197173355 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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e7758b533692596f140d527197173355
Registration Details
Taiwan FDA Registration: e7758b533692596f140d527197173355
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Device Details

"Artron" MICROALBUMIN TEST(Non-Sterile)
TW: "้›…ๅ‰ต" ๅพฎ็™ฝ่›‹็™ฝ่ฉฆๅŠ‘ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

e7758b533692596f140d527197173355

Ministry of Health Medical Device Import No. 018874

DHA09401887402

Company Information

Canada

Product Details

Limited to the first level of identification range of the Measures for the Administration of Medical Devices "Urine Protein or Albumin (Non-quantitative) Test System (A.1645)".

A Clinical chemistry and clinical toxicology

A1645 Urine protein or albumin (non-quantitative) test system

Imported from abroad

Dates and Status

Mar 07, 2018

Mar 07, 2023