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Senquin Piliklen Anti-K Immunoglobulin M Reagent - Taiwan Registration e85b54ec3c16e906f6433f366522e014

Access comprehensive regulatory information for Senquin Piliklen Anti-K Immunoglobulin M Reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e85b54ec3c16e906f6433f366522e014 and manufactured by SANQUIN REAGENTS B.V.. The authorized representative in Taiwan is METEK LAB INC..

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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e85b54ec3c16e906f6433f366522e014
Registration Details
Taiwan FDA Registration: e85b54ec3c16e906f6433f366522e014
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Device Details

Senquin Piliklen Anti-K Immunoglobulin M Reagent
TW: ๆฃฎๅฅŽๆฉ ็šฎ็†ๅ…‹ๅ€ซๆŠ—Kๅ…็–ซ็ƒ่›‹็™ฝM่ฉฆๅŠ‘
Risk Class 2

Registration Details

e85b54ec3c16e906f6433f366522e014

DHA00601639302

Company Information

Netherlands

Product Details

Hemotyping reagents used to detect the K (Kell) antigen on human red blood cells.

B Hematology, pathology, and genetics

B.4020 Analysis of specific tests

import

Dates and Status

Apr 19, 2006

Apr 19, 2026