Taiwan FDA registration 7fa1cffd890ed5db782ac4ae05a234d3

"Saibia" 3rd generation capillary electrophoresis instrument (unsterilized)

TW: "賽比亞"第三代毛細管電泳儀(未滅菌)
Taiwan flagTaiwan·Risk Class 1·SEBIA·Registered Oct 01, 2021 – Oct 31, 2025Expired
Registration details
Analysis ID
7fa1cffd890ed5db782ac4ae05a234d3
Customs Code
DHA08401509009
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 "Electrophoresis Equipment for Clinical Use (A.2485)" of the Measures for the Classification and Grading Management of Medical Equipment.
Product Type (Level 1)
A Clinical chemistry and clinical toxicology
Product Type (Level 2)
A.2485 Electrophoresis equipment for clinical use
Import Information
Input;; QMS/QSD
Dates and status
Registration Date
Oct 01, 2021
Expiry Date
Oct 31, 2025
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About this record

Access comprehensive regulatory information for "Saibia" 3rd generation capillary electrophoresis instrument (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 7fa1cffd890ed5db782ac4ae05a234d3 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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