Pure Global

Alpha Pregnancy Rapid Test Reagent - Taiwan Registration 38aaba740fa06584fe3376338f82fbf7

Access comprehensive regulatory information for Alpha Pregnancy Rapid Test Reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 38aaba740fa06584fe3376338f82fbf7 and manufactured by ALFA SCIENTIFIC DESIGNS, INC.. The authorized representative in Taiwan is RAFA INTERNATIONAL CORP..

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.

Free Database
Powered by Pure Global AI
89,000+ Devices
38aaba740fa06584fe3376338f82fbf7
Registration Details
Taiwan FDA Registration: 38aaba740fa06584fe3376338f82fbf7
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

Alpha Pregnancy Rapid Test Reagent
TW: ้˜ฟ็ˆพ็™ผๆ‡ทๅญ•ๅฟซ้€Ÿๆชขๆธฌ่ฉฆๅŠ‘
Risk Class 2

Registration Details

38aaba740fa06584fe3376338f82fbf7

DHA00601605600

Company Information

United States

Product Details

The Urine Pregnancy Rapid Test is a rapid, qualitative, single-step test for the measurement of chorionic gonadotropin (HCG) in human urine or serum as a diagnosis of early pregnancy.

A Clinical chemistry and clinical toxicology

A.1155 Human chorionic gonadotropin testing system

import

Dates and Status

Feb 27, 2006

Feb 27, 2026