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Beckman Coulter human IgG subtype detection reagent - Taiwan Registration 4c3b661e13e56e8cd43d85a162a1ffac

Access comprehensive regulatory information for Beckman Coulter human IgG subtype detection reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4c3b661e13e56e8cd43d85a162a1ffac and manufactured by SANQUIN REAGENTS B.V.. The authorized representative in Taiwan is BECKMAN COULTER TAIWAN INC., TAIWAN BRANCH (U.S.A.).

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4c3b661e13e56e8cd43d85a162a1ffac
Registration Details
Taiwan FDA Registration: 4c3b661e13e56e8cd43d85a162a1ffac
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Device Details

Beckman Coulter human IgG subtype detection reagent
TW: ่ฒๅ…‹ๆ›ผๅบซ็ˆพ็‰นไบบ้กžIgG ไบžๅž‹ๆชขๆธฌ่ฉฆๅŠ‘
Risk Class 2

Registration Details

4c3b661e13e56e8cd43d85a162a1ffac

DHA05603218404

Company Information

Netherlands

Product Details

This product is paired with Beckman IMMAGE/IMMAGE800 to quantitatively detect IgG subtypes in human serum and plasma.

C Immunology and Microbiology; A Clinical chemistry and clinical toxicology

C.5510 ๅ…็–ซ็ƒ่›‹็™ฝA,G,M,DๅŠEๅ…็–ซ่ฉฆ้ฉ—็ณป็ตฑ;; A.1150 ๆ กๆญฃๅ“;; A.1660 ๅ“็ฎกๆๆ–™(ๅˆ†ๆž่ˆ‡้žๅˆ†ๆž)

import

Dates and Status

Feb 21, 2019

Feb 21, 2029