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Bundis Human Immunoglobulin M Set - Taiwan Registration d17a68344f65d05c5b2e20bbe7072b80

Access comprehensive regulatory information for Bundis Human Immunoglobulin M Set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d17a68344f65d05c5b2e20bbe7072b80 and manufactured by THE BINDING SITE GROUP LIMITED. The authorized representative in Taiwan is EVERLIGHT BIOTECH(TAIWAN) CO., LTD..

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d17a68344f65d05c5b2e20bbe7072b80
Registration Details
Taiwan FDA Registration: d17a68344f65d05c5b2e20bbe7072b80
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Device Details

Bundis Human Immunoglobulin M Set
TW: ้‚ฆ่ฟชๆ–ฏไบบ้กžๅ…็–ซ็ƒ่›‹็™ฝMๅฅ—็ต„
Risk Class 2

Registration Details

d17a68344f65d05c5b2e20bbe7072b80

DHA00602410901

Company Information

United Kingdom

Product Details

Quantitative detection of immunoglobulin M (IgM) in human serum, heparin lithium plasma, or EDTA plasma is required in conjunction with a SPAPLUS analyzer.

C Immunology and microbiology

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

import

Dates and Status

Nov 05, 2012

Nov 05, 2027