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Saibia Immunofixation Electrophoresis Daratumumab Test Kit - Taiwan Registration 275f8a96690f31571dfabe2896924cec

Access comprehensive regulatory information for Saibia Immunofixation Electrophoresis Daratumumab Test Kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 275f8a96690f31571dfabe2896924cec and manufactured by SEBIA. The authorized representative in Taiwan is ARQon Medtech Co., Ltd..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including SEBIA, and 1 recent registrations in the same category. 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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275f8a96690f31571dfabe2896924cec
Registration Details
Taiwan FDA Registration: 275f8a96690f31571dfabe2896924cec
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Device Details

Saibia Immunofixation Electrophoresis Daratumumab Test Kit
TW: ่ณฝๆฏ”ไบž ๅ…็–ซๅ›บๅฎš้›ปๆณณDaratumumabๆชขๆธฌๅฅ—็ต„
Risk Class 2

Registration Details

275f8a96690f31571dfabe2896924cec

DHA05603466708

Company Information

France

Product Details

This product is paired with HYDRAGEL IF detection reagent and semi-automated HYDRASYS 2 electrophoresis equipment, HYDRAGEL IF detects monoclonal antibodies in human serum by immunofixation electrophoresis.

C Immunology and microbiology

C.5510 ๅ…็–ซ็ƒ่›‹็™ฝA,G,M,DๅŠEๅ…็–ซ่ฉฆ้ฉ—็ณป็ตฑ

QMS/QSD;; ่ผธๅ…ฅ

Dates and Status

Jun 24, 2021

Jun 24, 2026

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