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"WEIYOU" Ovulation Test (Non-Sterile) - Taiwan Registration 805554963fa2ac36e622eb8cb187593f

Access comprehensive regulatory information for "WEIYOU" Ovulation 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 805554963fa2ac36e622eb8cb187593f and manufactured by SPD SWISS PRECISION DIAGNOSTICS GMBH. The authorized representative in Taiwan is WEIYOU TECH INC..

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805554963fa2ac36e622eb8cb187593f
Registration Details
Taiwan FDA Registration: 805554963fa2ac36e622eb8cb187593f
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Device Details

"WEIYOU" Ovulation Test (Non-Sterile)
TW: "ๅพฎๅ‹" ๆŽ’ๅตๆธฌ่ฉฆ็ญ† (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

805554963fa2ac36e622eb8cb187593f

Ministry of Health Medical Device Import No. 022337

DHA09402233704

Company Information

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

Imported from abroad

Dates and Status

Feb 25, 2021

Feb 25, 2026