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Reagent for Mitsubishi immunoglobulin M assay - Taiwan Registration e7f2e489ca19ca4a4431f688118aa413

Access comprehensive regulatory information for Reagent for Mitsubishi immunoglobulin M assay in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e7f2e489ca19ca4a4431f688118aa413 and manufactured by MITSUBISHI KAGAKU IATRON. INC.. The authorized representative in Taiwan is Jingxiang 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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e7f2e489ca19ca4a4431f688118aa413
Registration Details
Taiwan FDA Registration: e7f2e489ca19ca4a4431f688118aa413
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Device Details

Reagent for Mitsubishi immunoglobulin M assay
TW: ไธ‰่ฑๅ…็–ซ็ƒ่›‹็™ฝMๆธฌๅฎš็”จ่ฉฆๅŠ‘
Risk Class 2
Cancelled

Registration Details

e7f2e489ca19ca4a4431f688118aa413

DHA00601719503

Company Information

Product Details

The haze of immunoglobulin M (IgM) in serum was analyzed.

C Immunology and microbiology

C.5510 ๅ…็–ซ็ƒ่›‹็™ฝA,G,M,DๅŠEๅ…็–ซ่ฉฆ้ฉ—็ณป็ตฑ

import

Dates and Status

Jul 05, 2006

Jul 05, 2011

Oct 30, 2012

Cancellation Information

Logged out

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