Taiwan FDA registration 88687129b35b8b8376c0f199eba91ec6

Saibia Immunofixation Electrophoresis Daratumumab Test Kit

TW: 賽比亞 免疫固定電泳Daratumumab檢測套組
Taiwan flagTaiwan·Risk Class 2·SEBIA·Registered Jun 24, 2021 – Jun 24, 2026Expired
Registration details
Analysis ID
88687129b35b8b8376c0f199eba91ec6
Customs Code
DHA05603466708
Company information
Manufacturer
SEBIA
Manufacturer Country
France
Authorized Representative
SCN TRADING COMPANY LIMITED
Product details
Intended Use
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.
Product Type (Level 1)
C Immunology and microbiology
Product Type (Level 2)
C.5510 免疫球蛋白A,G,M,D及E免疫試驗系統
Import Information
QMS/QSD;; 輸入
Dates and status
Registration Date
Jun 24, 2021
Expiry Date
Jun 24, 2026
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About this record

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 88687129b35b8b8376c0f199eba91ec6 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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