Taiwan FDA registration 26cde3cbd4f867ba4fb16696499d4961
Wistron Rapid Reagent Reader (Unsterilized)
TW: “緯創” 快速試劑判讀儀 (未滅菌)
Taiwan·Risk Class 1·WISTRON CORPORATION·Registered Apr 28, 2020 – Apr 28, 2025ExpiredRegistration details
- Analysis ID
- 26cde3cbd4f867ba4fb16696499d4961
Company information
- Manufacturer
- WISTRON CORPORATION
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- WISTRON CORPORATION
Product details
- Intended Use
- Limited to the first level of identification range of "density meter/scanner for clinical use (integration, reflection, thin layer chromolayer or radioactive chromolayer analysis)" (A.2400) 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.2400 Density Meter/Sweeper for Clinical Use (Separation, Reflection, Thin Layer or Radioactive Color Layer Analysis)
- Import Information
- 國產;; QMS/QSD
Dates and status
- Registration Date
- Apr 28, 2020
- Expiry Date
- Apr 28, 2025
About this record
Access comprehensive regulatory information for Wistron Rapid Reagent Reader (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 26cde3cbd4f867ba4fb16696499d4961 and manufactured by WISTRON CORPORATION. The authorized representative in Taiwan is WISTRON CORPORATION.
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