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"ARTRON" FSH TEST (Non-Sterile) - Taiwan Registration 923254d847376d7bf301121047c68b12

Access comprehensive regulatory information for "ARTRON" FSH 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 923254d847376d7bf301121047c68b12 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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923254d847376d7bf301121047c68b12
Registration Details
Taiwan FDA Registration: 923254d847376d7bf301121047c68b12
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Device Details

"ARTRON" FSH TEST (Non-Sterile)
TW: "้›…ๆ˜Œ"ๅตๆณกๅˆบๆฟ€ๆฟ€็ด ๆชขๆธฌ่ฉฆๅŠ‘ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

923254d847376d7bf301121047c68b12

Ministry of Health Medical Device Import No. 016209

DHA09401620909

Company Information

Canada

Product Details

Limited to the first level recognition range of the follicle-stimulating hormone test system (A.1300) of the management method of medical equipment.

A Clinical chemistry and clinical toxicology

A1300 Follicle-stimulating hormone testing system

Imported from abroad

Dates and Status

Mar 01, 2016

Mar 01, 2026