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“Vircell” CYTOMEGALOVIRUS VIRCLIA IgG MONOTEST - Taiwan Registration 8a1daadefed2760c2bfa321d1e6650de

Access comprehensive regulatory information for “Vircell” CYTOMEGALOVIRUS VIRCLIA IgG MONOTEST in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8a1daadefed2760c2bfa321d1e6650de and manufactured by VIRCELL, S.L. The authorized representative in Taiwan is Abbott Rapid Diagnostics Health Corp..

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8a1daadefed2760c2bfa321d1e6650de
Registration Details
Taiwan FDA Registration: 8a1daadefed2760c2bfa321d1e6650de
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Device Details

“Vircell” CYTOMEGALOVIRUS VIRCLIA IgG MONOTEST
TW: “凡賽爾”巨細胞病毒化學冷光免疫分析IgG試劑組
Risk Class 2
MD

Registration Details

8a1daadefed2760c2bfa321d1e6650de

Ministry of Health Medical Device Import No. 031451

DHA05603145109

Company Information

Spain

Product Details

This product is an indirect chemiluminescent immunoassay (CLIA) reagent with ThunderBolt Analyzer. Detection of IgG antibodies to cytomegalovirus in human plasma.

C Immunology and microbiology devices

C3175 CMV serum reagent

Imported from abroad

Dates and Status

Sep 05, 2018

Sep 05, 2023