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Sebia Gel protein electrophoresis detection reagent (unsterilized) - Taiwan Registration 1d4c762cc4e19e2b3862035b314779b9

Access comprehensive regulatory information for Sebia Gel protein electrophoresis detection reagent (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 1d4c762cc4e19e2b3862035b314779b9 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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1d4c762cc4e19e2b3862035b314779b9
Registration Details
Taiwan FDA Registration: 1d4c762cc4e19e2b3862035b314779b9
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Device Details

Sebia Gel protein electrophoresis detection reagent (unsterilized)
TW: ่ณฝๆฏ”ไบž ๅ‡่† ่›‹็™ฝ้›ปๆณณๆชขๆธฌ่ฉฆๅŠ‘(ๆœชๆป…่Œ)
Risk Class 1

Registration Details

1d4c762cc4e19e2b3862035b314779b9

DHA09402270000

Company Information

France

Product Details

Limited to the first level identification range of the classification and grading management method of medical equipment, protein (chemical separation method) test system (A.1630).

A Clinical chemistry and clinical toxicology

A.1630 Protein (Chemical Separation) Test System

Input;; QMS/QSD

Dates and Status

Nov 16, 2021

Nov 16, 2026

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