Taiwan FDA registration 1220c2371478f1dcdba80cf403a32f31

"Daislin" Reasan Automatic Biochemical Analyzer (Unsterilized)

TW: "戴思林" 禮亞尚 全自動生化分析儀 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·DIASORIN DEUTSCHLAND GMBH·Registered Oct 01, 2021 – Oct 31, 2022Cancelled
Registration details
Analysis ID
1220c2371478f1dcdba80cf403a32f31
Customs Code
DHA08401122104
Company information
Manufacturer Country
Germany
Authorized Representative
EVERLIGHT BIOTECH(TAIWAN) CO., LTD.
Product details
Intended Use
Limited to the first level identification range of the "Individual Photometric Chemical Analyzer for Clinical Use (A.2160)" of the Measures for the Administration 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
Import Information
QMS/QSD;; 輸入
Dates and status
Registration Date
Oct 01, 2021
Expiry Date
Oct 31, 2022
Cancellation Date
Feb 01, 2023
Cancellation information
Status
Logged out
Reason
未展延而逾期者
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About this record

Access comprehensive regulatory information for "Daislin" Reasan Automatic Biochemical 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 1220c2371478f1dcdba80cf403a32f31 and manufactured by DIASORIN DEUTSCHLAND GMBH. The authorized representative in Taiwan is EVERLIGHT BIOTECH(TAIWAN) CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including DIASORIN DEUTSCHLAND GMBH, 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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