"Baqi" Bayer Flexion Cold Light Meter (Unsterilized)
Taiwan·Risk Class 1·BIOKIT, S.A.·Registered Dec 17, 2012 – Dec 17, 2022Cancelled- Analysis ID
- 3b295c2c81d728e6d7a2843715727d82
- Customs Code
- DHA04401249204
- Manufacturer
- BIOKIT, S.A.
- Manufacturer Country
- Spain
- Authorized Representative
- TRUGENE DIAGNOSTICS, INC.
- Intended Use
- Limited to the first level identification range of "Colorimeter, Photometer or Spectrophotometer for Clinical Use (A.2300)" under the Measures for the Administration of Medical Devices.
- 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
- Dec 17, 2012
- Expiry Date
- Dec 17, 2022
- Cancellation Date
- Sep 30, 2021
- Status
- Logged out
- Reason
- 轉為登錄字號
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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 3b295c2c81d728e6d7a2843715727d82 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.