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Fukushima Quick Fetch A Fetal Globulin Rapid Assay Reagent - Taiwan Registration a4a25edbcd08b789f551521a36e97495

Access comprehensive regulatory information for Fukushima Quick Fetch A Fetal Globulin Rapid Assay Reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a4a25edbcd08b789f551521a36e97495 and manufactured by VEDA LAB. The authorized representative in Taiwan is Fukushima Medical Equipment Co., Ltd.

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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a4a25edbcd08b789f551521a36e97495
Registration Details
Taiwan FDA Registration: a4a25edbcd08b789f551521a36e97495
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Device Details

Fukushima Quick Fetch A Fetal Globulin Rapid Assay Reagent
TW: ็ฆๅณถๅฟซๅ–็”ฒๅž‹่ƒŽๅ…’็ƒ่›‹็™ฝๅฟซ้€Ÿๆธฌๅฎš่ฉฆๅŠ‘
Risk Class 2
Cancelled

Registration Details

a4a25edbcd08b789f551521a36e97495

DHA00601638605

Company Information

France

Product Details

Qualitative detection of alpha-fetal globulin in human whole blood, plasma, and serum.

C Immunology and microbiology

C.6010 ่…ซ็˜ค็›ธ้—œๆŠ—ๅŽŸๅ…็–ซ่ฉฆ้ฉ—็ณป็ตฑ

import

Dates and Status

Apr 19, 2006

Apr 19, 2011

Nov 20, 2012

Cancellation Information

Logged out

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