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"IF" Follicular Stimulating Hormone (FSH) Rapid Test (Non-Sterile) - Taiwan Registration 41fbce907fc2538a50e7116ee50cbe3e

Access comprehensive regulatory information for "IF" Follicular Stimulating Hormone (FSH) Rapid 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 41fbce907fc2538a50e7116ee50cbe3e and manufactured by FIRSTEP BIORESEARCH INC.. The authorized representative in Taiwan is FIRSTEP BIORESEARCH INC..

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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41fbce907fc2538a50e7116ee50cbe3e
Registration Details
Taiwan FDA Registration: 41fbce907fc2538a50e7116ee50cbe3e
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Device Details

"IF" Follicular Stimulating Hormone (FSH) Rapid Test (Non-Sterile)
TW: โ€œไพ่Š™โ€ๅตๆณกๅˆบๆฟ€ๆฟ€็ด ๆชขๆธฌ่ฉฆๅŠ‘ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

41fbce907fc2538a50e7116ee50cbe3e

Ministry of Health Medical Device Manufacturing No. 007508

Company Information

Taiwan, Province of China

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

Produced in Taiwan, China

Dates and Status

Oct 31, 2018

Oct 31, 2023