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Remai dysentery amoeba test panel - Taiwan Registration 9b330dcca0795217d364ae60b17d35ad

Access comprehensive regulatory information for Remai dysentery amoeba test panel in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9b330dcca0795217d364ae60b17d35ad and manufactured by REMEL EUROPE LIMITED. The authorized representative in Taiwan is Qixin Biotechnology 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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9b330dcca0795217d364ae60b17d35ad
Registration Details
Taiwan FDA Registration: 9b330dcca0795217d364ae60b17d35ad
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Device Details

Remai dysentery amoeba test panel
TW: ้Šณ้‚ ็—ข็–พ้˜ฟ็ฑณๅทดๆชข้ฉ—่ฉฆๅŠ‘็ต„
Risk Class 1
Cancelled

Registration Details

9b330dcca0795217d364ae60b17d35ad

DHA04400426500

Company Information

United Kingdom

Product Details

็”จๆ–ผๅฎšๆ€งๅตๆธฌไบบ้กž็ณžไพฟไน‹่ƒๅ–ๆถฒไธญไน‹็—ข็–พ้˜ฟ็ฑณๅทดๅฐˆไธ€ๆ€งๆŠ—ๅŽŸ(Entamoeba histolytica specific antigen, EHSA).

C Immunology and microbiology

C.3220 ็—ข็–พ้˜ฟ็ฑณๅทด่ก€ๆธ…่ฉฆๅŠ‘

import

Dates and Status

Apr 28, 2006

Apr 28, 2011

Nov 08, 2012

Cancellation Information

Logged out

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