Taiwan FDA registration 126227fb3c757ec5ecb72348926c18bd

Reashan Laboratory Automation System Chemical Cold Light Immunoassay Analyzer (Unsterilized)

TW: 禮亞尚實驗室自動化系統化學冷光免疫分析儀(未滅菌)

Taiwan·Risk Class 1·DiaSorin Italia SpA·Registered Oct 08, 2021 – Oct 31, 2025Expired

Registration details

Analysis ID: 126227fb3c757ec5ecb72348926c18bd
Customs Code: DHA084a0000405

Company information

Manufacturer: DiaSorin Italia SpA
Manufacturer Country: Italy
Authorized Representative: EVERLIGHT BIOTECH(TAIWAN) CO., LTD.

Product details

Intended Use: Limited to the first level identification range of the "Individual Photometric Chemistry Analyzer for Clinical Use (A.2160)" of the Measures for the Classification and Grading of Medical Devices.
Product Type (Level 1): A Clinical chemistry and clinical toxicology
Product Type (Level 2): A.2160 Individual Photometric Chemistry Analyzer for Clinical Use

Dates and status

Registration Date: Oct 08, 2021
Expiry Date: Oct 31, 2025

About this record

Access comprehensive regulatory information for Reashan Laboratory Automation System Chemical Cold Light Immunoassay Analyzer (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 126227fb3c757ec5ecb72348926c18bd and manufactured by DiaSorin Italia SpA. The authorized representative in Taiwan is EVERLIGHT BIOTECH(TAIWAN) CO., LTD..

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