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ASK Ketamine Rapid Test - Taiwan Registration 813f87d2684385c441b84d69d82fdc32

Access comprehensive regulatory information for ASK Ketamine Rapid Test in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 813f87d2684385c441b84d69d82fdc32 and manufactured by TONYAR BIOTECH. INC.. The authorized representative in Taiwan is TONYAR 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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813f87d2684385c441b84d69d82fdc32
Registration Details
Taiwan FDA Registration: 813f87d2684385c441b84d69d82fdc32
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Device Details

ASK Ketamine Rapid Test
TW: ๆฑ่€€ๆ„ทไป–ๅ‘ฝๅฟซ้€Ÿๆชข้ฉ—่ฉฆๅŠ‘
Risk Class 2
MD

Registration Details

813f87d2684385c441b84d69d82fdc32

Ministry of Health Medical Device Manufacturing No. 004704

Company Information

Taiwan, Province of China

Product Details

Competitive immunochromatography to qualitatively detect the presence of katamine in human urine (Ketamine, KET, Ktamine, ketamine)

A Clinical chemistry and clinical toxicology

A0001 Phencyclidine Test System

Produced in Taiwan, China

Dates and Status

Aug 06, 2014

Aug 06, 2024