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IF Ovulation(LH) Rapid Test (Non-sterile) - Taiwan Registration f002cf0739ec0c5ab00215bd0cc4f355

Access comprehensive regulatory information for IF Ovulation(LH) 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 f002cf0739ec0c5ab00215bd0cc4f355 and manufactured by FIRSTEP BIORESEARCH INC.. The authorized representative in Taiwan is FIRSTEP BIORESEARCH INC..

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f002cf0739ec0c5ab00215bd0cc4f355
Registration Details
Taiwan FDA Registration: f002cf0739ec0c5ab00215bd0cc4f355
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Device Details

IF Ovulation(LH) Rapid Test (Non-sterile)
TW: ไพ่Š™ ๆŽ’ๅตๆชขๆธฌ่ฉฆๅŠ‘ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

f002cf0739ec0c5ab00215bd0cc4f355

Ministry of Health Medical Device Manufacturing No. 006605

Company Information

Taiwan, Province of China

Product Details

Limited to the first level recognition range of the "Luteinizing hormone test system (A.1485)" of the Measures for the Administration of Medical Devices.

A Clinical chemistry and clinical toxicology

A1485 Progesterone Test System

Produced in Taiwan, China

Dates and Status

Feb 23, 2017

Feb 23, 2027