Taiwan FDA registration 0d77784d156f90174a89d9976785a7d9
Beckman Coulter High Performance Arthurs Immunoassay System (Unsterilized)
TW: 貝克曼庫爾特 高效能亞瑟斯免疫分析系統 (未滅菌)
Registration details
- Analysis ID
- 0d77784d156f90174a89d9976785a7d9
- Customs Code
- DHA084a0006703
Company information
- Manufacturer
- BECKMAN COULTER, INC.
- Manufacturer Country
- United States
- Authorized Representative
- BECKMAN COULTER TAIWAN INC., TAIWAN BRANCH (U.S.A.)
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
- May 21, 2022
- Expiry Date
- Oct 31, 2025
About this record
Access comprehensive regulatory information for Beckman Coulter High Performance Arthurs Immunoassay System (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 0d77784d156f90174a89d9976785a7d9 and manufactured by BECKMAN COULTER, INC.. The authorized representative in Taiwan is BECKMAN COULTER TAIWAN INC., TAIWAN BRANCH (U.S.A.).
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