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"SPD" Clearblue Ovulation Test (Non-Sterile) - Taiwan Registration 4cf0f31a903c63363630ae506dc76472

Access comprehensive regulatory information for "SPD" Clearblue 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 4cf0f31a903c63363630ae506dc76472 and manufactured by SPD Swiss Precision Diagnostics GmbH. The authorized representative in Taiwan is SUNGYIN BIO INTERNATIONAL CO., LTD..

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4cf0f31a903c63363630ae506dc76472
Registration Details
Taiwan FDA Registration: 4cf0f31a903c63363630ae506dc76472
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Device Details

"SPD" Clearblue Ovulation Test (Non-Sterile)
TW: "้€Ÿๅฟ…ๅพ—"ๆŽ’ๅตๆธฌ่ฉฆ็ญ†(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

4cf0f31a903c63363630ae506dc76472

Ministry of Health Medical Device Import No. 019258

DHA09401925801

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

Jul 03, 2018

Jul 03, 2023