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Kwai Ke Quick Know Pregnancy Test Pen - Taiwan Registration 917583f23bfb38d1c0d638dad0a93e01

Access comprehensive regulatory information for Kwai Ke Quick Know Pregnancy Test Pen in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 917583f23bfb38d1c0d638dad0a93e01 and manufactured by PHAMATECH, INC. The authorized representative in Taiwan is GLOW STAR BIOTECH 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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917583f23bfb38d1c0d638dad0a93e01
Registration Details
Taiwan FDA Registration: 917583f23bfb38d1c0d638dad0a93e01
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Device Details

Kwai Ke Quick Know Pregnancy Test Pen
TW: ่‘ตๅ…‹ๅฟซ็Ÿฅ ้ฉ—ๅญ•็ญ†
Risk Class 2

Registration Details

917583f23bfb38d1c0d638dad0a93e01

DHA00601904701

Company Information

United States

Product Details

Detection of human chorionic gonadotropin hCG in urine as a test for early diagnosis of pregnancy.

A Clinical chemistry and clinical toxicology

A.1155 Human chorionic gonadotropin testing system

import

Dates and Status

May 16, 2008

May 16, 2023