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“Immucor” Anti-A series 1 - Taiwan Registration 8ec05451ed3ca6843fe453e7d8cdb0dc

Access comprehensive regulatory information for “Immucor” Anti-A series 1 in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 8ec05451ed3ca6843fe453e7d8cdb0dc and manufactured by IMMUCOR, INC.. The authorized representative in Taiwan is Y.H. BIOTEK 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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8ec05451ed3ca6843fe453e7d8cdb0dc
Registration Details
Taiwan FDA Registration: 8ec05451ed3ca6843fe453e7d8cdb0dc
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Device Details

“Immucor” Anti-A series 1
TW: “依免可”抗A血清(系列1)
Risk Class 3
MD

Registration Details

8ec05451ed3ca6843fe453e7d8cdb0dc

Ministry of Health Medical Device Import No. 025261

DHA05602526105

Company Information

United States

Product Details

Identification of blood group A, suitable for slide, tube and microdisc testing.

B Hematology and pathology devices

B4020 Analyze specific reagents

Imported from abroad

Dates and Status

Aug 13, 2013

Aug 13, 2028