Taiwan FDA registration d401b255f5833647cd6a603462b6a4be
"Canon" automatic biochemistry analyzer (unsterilized)
TW: "佳能"自動生化分析儀(未滅菌)
Taiwan·Risk Class 1·CANON MEDICAL SYSTEMS CORPORATION·Registered Oct 01, 2021 – Oct 31, 2025ExpiredRegistration details
- Analysis ID
- d401b255f5833647cd6a603462b6a4be
- Customs Code
- DHA08401919902
Company information
- Manufacturer
- CANON MEDICAL SYSTEMS CORPORATION
- Manufacturer Country
- Japan
- Authorized Representative
- TUNYEN ENTERPRISE CORPORATION
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
- import
Dates and status
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2025
About this record
Access comprehensive regulatory information for "Canon" automatic biochemistry 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 d401b255f5833647cd6a603462b6a4be and manufactured by CANON MEDICAL SYSTEMS CORPORATION. The authorized representative in Taiwan is TUNYEN ENTERPRISE CORPORATION.
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