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INNO-LiPA HLA-DRB decorder Amplification - Taiwan Registration 77c3de629109ee9e4d1bb085ccde27c1

Access comprehensive regulatory information for INNO-LiPA HLA-DRB decorder Amplification in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 77c3de629109ee9e4d1bb085ccde27c1 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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77c3de629109ee9e4d1bb085ccde27c1
Registration Details
Taiwan FDA Registration: 77c3de629109ee9e4d1bb085ccde27c1
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Device Details

INNO-LiPA HLA-DRB decorder Amplification
TW: ๅ› ่ซพ-็ซ‹ๅธ•ไบบ้กž็™ฝ่ก€็ƒๆŠ—ๅŽŸๆ“ดๅขž่ฉฆๅŠ‘็ต„-DRBไฝ้ปžๅˆ†ๆž
Risk Class 2
MD
Cancelled

Registration Details

77c3de629109ee9e4d1bb085ccde27c1

Ministry of Health Medical Device Import No. 027535

DHA05602753500

Company Information

Belgium

Product Details

B Hematology and pathology devices

B0001 Human leukocyte antigen segmentation board

Imported from abroad

Dates and Status

Jul 28, 2015

Jul 28, 2025

Oct 28, 2022

Cancellation Information

Logged out

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