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INNO-LiPA HLA-DRB1 Plus - Taiwan Registration d03c92074f13d50e6380bece878168f2

Access comprehensive regulatory information for INNO-LiPA HLA-DRB1 Plus in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d03c92074f13d50e6380bece878168f2 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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d03c92074f13d50e6380bece878168f2
Registration Details
Taiwan FDA Registration: d03c92074f13d50e6380bece878168f2
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Device Details

INNO-LiPA HLA-DRB1 Plus
TW: ๅ› ่ซพ-็ซ‹ๅธ•ๆ ธ้…ธๆŽข้‡ๅผไบบ้กž็™ฝ่ก€็ƒๆŠ—ๅŽŸ่ฉฆๅŠ‘็ต„-DRB1ไฝ้ปž
Risk Class 2
MD
Cancelled

Registration Details

d03c92074f13d50e6380bece878168f2

Ministry of Health Medical Device Import No. 027531

DHA05602753105

Company Information

Belgium

Product Details

B Hematology and pathology devices

B0001 Human leukocyte antigen segmentation board

Imported from abroad

Dates and Status

Jul 21, 2015

Jul 21, 2025

Oct 28, 2022

Cancellation Information

Logged out

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