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INNO-LiPA HLA-DQB1 MultiPlex - Taiwan Registration e2d727f773c7393d13af0383ca4b907a

Access comprehensive regulatory information for INNO-LiPA HLA-DQB1 MultiPlex in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e2d727f773c7393d13af0383ca4b907a and manufactured by FUJIREBIO EUROPE N.V.. The authorized representative in Taiwan is Taiwan Fu Pharmaceutical 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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e2d727f773c7393d13af0383ca4b907a
Registration Details
Taiwan FDA Registration: e2d727f773c7393d13af0383ca4b907a
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Device Details

INNO-LiPA HLA-DQB1 MultiPlex
TW: ๅ› ่ซพ-็ซ‹ๅธ•ไบบ้กž็™ฝ่ก€็ƒๆŠ—ๅŽŸๆ“ดๅขž่ฉฆๅŠ‘็ต„-DQB1ไฝ้ปž
Risk Class 2
MD
Cancelled

Registration Details

e2d727f773c7393d13af0383ca4b907a

Ministry of Health Medical Device Import No. 027533

DHA05602753309

Company Information

Belgium

Product Details

B Hematology and pathology devices

B0001 Human leukocyte antigen segmentation board

Imported from abroad

Dates and Status

Jul 23, 2015

Jul 23, 2025

Oct 28, 2022

Cancellation Information

Logged out

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