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INNO-LiPA HLA-A MultiPlex - Taiwan Registration 294258335dc81b44ec6a8d1335d6c37f

Access comprehensive regulatory information for INNO-LiPA HLA-A MultiPlex in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 294258335dc81b44ec6a8d1335d6c37f 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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294258335dc81b44ec6a8d1335d6c37f
Registration Details
Taiwan FDA Registration: 294258335dc81b44ec6a8d1335d6c37f
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Device Details

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

Registration Details

294258335dc81b44ec6a8d1335d6c37f

Ministry of Health Medical Device Import No. 027363

DHA05602736300

Company Information

Belgium

Product Details

B Hematology and pathology devices

B0001 Human leukocyte antigen segmentation board

Imported from abroad

Dates and Status

Jun 30, 2015

Jun 30, 2025

Oct 28, 2022

Cancellation Information

Logged out

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