Taiwan FDA registration 2466139490d47fbb8a376a94c3f704cb

"Sabia" automatic capillary electrophoresis instrument (unsterilized)

TW: 〝賽比亞〞全自動毛細管電泳儀 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·SEBIA·Registered Jan 09, 2012 – Jan 09, 2022Cancelled
Registration details
Analysis ID
2466139490d47fbb8a376a94c3f704cb
Customs Code
DHA04401128000
Company information
Manufacturer
SEBIA
Manufacturer Country
France
Authorized Representative
SCN TRADING COMPANY LIMITED
Product details
Intended Use
Limited to the first level identification scope of "Electrophoresis Equipment for Clinical Use (A.2485)" under the Measures for the Administration of Medical Devices.
Product Type (Level 1)
A Clinical chemistry and clinical toxicology
Product Type (Level 2)
A.2485 Electrophoresis equipment for clinical use
Import Information
QMS/QSD;; 輸入
Dates and status
Registration Date
Jan 09, 2012
Expiry Date
Jan 09, 2022
Cancellation Date
Sep 30, 2021
Cancellation information
Status
Logged out
Reason
轉為登錄字號
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About this record

Access comprehensive regulatory information for "Sabia" automatic 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 2466139490d47fbb8a376a94c3f704cb 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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