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Fukushima Kotake pylori rapid assay reagent - Taiwan Registration 514611e2825f4e2747f742279809f6ed

Access comprehensive regulatory information for Fukushima Kotake pylori rapid assay reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 514611e2825f4e2747f742279809f6ed 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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514611e2825f4e2747f742279809f6ed
Registration Details
Taiwan FDA Registration: 514611e2825f4e2747f742279809f6ed
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Device Details

Fukushima Kotake pylori rapid assay reagent
TW: ็ฆๅณถๅฟซๅ–ๅนฝ้–€ๆกฟ่Œๅฟซ้€Ÿๆธฌๅฎš่ฉฆๅŠ‘
Risk Class 1
Cancelled

Registration Details

514611e2825f4e2747f742279809f6ed

DHA04400230400

Company Information

France

Product Details

Qualitative detection of Helicobacter pylori IgG antibodies in human whole blood, plasma, and serum.

C Immunology and microbiology

C.0003 ่žบๆ—‹ๆกฟ่Œๅฑฌ่ก€ๆธ…่ฉฆๅŠ‘

import

Dates and Status

Dec 22, 2005

Dec 22, 2010

Nov 20, 2012

Cancellation Information

Logged out

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