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Saibia Third generation capillary heme detection reagent - Taiwan Registration 972584b8db63198a5060331967ad5615

Access comprehensive regulatory information for Saibia Third generation capillary heme detection reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 972584b8db63198a5060331967ad5615 and manufactured by SEBIA. The authorized representative in Taiwan is SCN TRADING COMPANY LIMITED.

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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972584b8db63198a5060331967ad5615
Registration Details
Taiwan FDA Registration: 972584b8db63198a5060331967ad5615
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Device Details

Saibia Third generation capillary heme detection reagent
TW: ่ณฝๆฏ”ไบž ็ฌฌไธ‰ไปฃๆฏ›็ดฐ็ฎก่ก€็ด…็ด ๆชขๆธฌ่ฉฆๅŠ‘
Risk Class 2

Registration Details

972584b8db63198a5060331967ad5615

DHA05603294401

Company Information

France

Product Details

This product uses capillary electrophoresis to isolate normal heme (A, F and A2) in an alkaline buffer (pH 9.4) and detect the main variants of heme (S, C, E, and D). SUITABLE FOR SEBIA CAPILLARYS 3 INSTRUMENTS.

B Hematology, pathology, and genetics

B.7440 Heme electrophoresis analysis system

import

Dates and Status

Oct 17, 2019

Oct 17, 2029

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