Taiwan FDA registration c21cddd0d60fdb1fe5c2987f1c8b0b8f
"Reashan" Automatic Cold Light Immunity Analyzer (Unsterilized)
TW: “禮亞尚” 全自動冷光免疫分析儀(未滅菌)
Taiwan·Risk Class 1·DIASORIN S.P.A.·Registered Oct 01, 2021 – Oct 31, 2025ExpiredRegistration details
- Analysis ID
- c21cddd0d60fdb1fe5c2987f1c8b0b8f
- Customs Code
- DHA08402180102
Company information
- Manufacturer
- DIASORIN S.P.A.
- 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
- Import Information
- Input;; QMS/QSD
Dates and status
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2025
About this record
Access comprehensive regulatory information for "Reashan" Automatic Cold Light Immunity 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 c21cddd0d60fdb1fe5c2987f1c8b0b8f and manufactured by DIASORIN S.P.A.. The authorized representative in Taiwan is EVERLIGHT BIOTECH(TAIWAN) CO., LTD..
This page provides complete technical specifications, regulatory compliance details. 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.
Free DatabasePowered by Pure Global AI89,000+ Devices