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“Immucor” Anti-Jkb (Monoclonal) Gamma-clone - Taiwan Registration 1748f3620e17433ae50c7bfede75a4e4

Access comprehensive regulatory information for “Immucor” Anti-Jkb (Monoclonal) Gamma-clone in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1748f3620e17433ae50c7bfede75a4e4 and manufactured by IMMUCOR, INC.. The authorized representative in Taiwan is Y.H. BIOTEK CO., LTD..

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1748f3620e17433ae50c7bfede75a4e4
Registration Details
Taiwan FDA Registration: 1748f3620e17433ae50c7bfede75a4e4
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Device Details

“Immucor” Anti-Jkb (Monoclonal) Gamma-clone
TW: “依免可” 單株抗體抗Jkb血型試劑
Risk Class 2
MD

Registration Details

1748f3620e17433ae50c7bfede75a4e4

Ministry of Health Medical Device Import No. 027539

DHA05602753908

Company Information

United States

Product Details

It is suitable for the detection of red blood cell Jkb (Jk2) antigen in test by test in vitro test.

B Hematology and pathology devices

B4020 Analyze specific reagents

Imported from abroad

Dates and Status

Jul 29, 2015

Jul 29, 2025