"Baqi" Bayer Flexion Cold Light Meter (Unsterilized)
Taiwan·Risk Class 1·BIOKIT, S.A.·Registered Oct 01, 2021 – Oct 31, 2025Expired- Analysis ID
- a46f097e1700f6521f44b9181934e39e
- Customs Code
- DHA08401249201
- Manufacturer
- BIOKIT, S.A.
- Manufacturer Country
- Spain
- Authorized Representative
- TRUGENE DIAGNOSTICS, INC.
- Intended Use
- Limited to the first level identification range of the Measures for the Classification and Grading of Medical Devices "Colorimeter, Photometer or Spectrophotometer for Clinical Use (A.2300)".
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.2300 Colorimeter, photometer, or spectrophotometer for clinical use
- Import Information
- QMS/QSD;; 輸入
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2025
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Access comprehensive regulatory information for "Baqi" Bayer Flexion Cold Light Meter (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a46f097e1700f6521f44b9181934e39e and manufactured by BIOKIT, S.A.. The authorized representative in Taiwan is TRUGENE DIAGNOSTICS, INC..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including BIOKIT, S.A., 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.