Taiwan FDA registration 2ccee5cf7dd3f6acd32d422707f0994a

Sebia Gel protein electrophoresis detection reagent (unsterilized)

TW: 賽比亞 凝膠蛋白電泳檢測試劑(未滅菌)
Taiwan flagTaiwan·Risk Class 1·SEBIA·Registered Nov 16, 2021 – Nov 16, 2026Active
Registration details
Analysis ID
2ccee5cf7dd3f6acd32d422707f0994a
Customs Code
DHA09402270000
Company information
Manufacturer
SEBIA
Manufacturer Country
France
Authorized Representative
SCN TRADING COMPANY LIMITED
Product details
Intended Use
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).
Product Type (Level 1)
A Clinical chemistry and clinical toxicology
Product Type (Level 2)
A.1630 Protein (Chemical Separation) Test System
Import Information
QMS/QSD;; 輸入
Dates and status
Registration Date
Nov 16, 2021
Expiry Date
Nov 16, 2026
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About this record

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 2ccee5cf7dd3f6acd32d422707f0994a 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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