"Burry" Spectrophotometer for Clinical Use (Unsterilized)
Taiwan·Risk Class 1·BIO-RAD·Registered Sep 13, 2017 – Sep 13, 2022Cancelled- Analysis ID
- be4de7358252e2011dd1cd02f3f2510b
- Customs Code
- DHA09401830900
- Manufacturer
- BIO-RAD
- Manufacturer Country
- France
- Authorized Representative
- Bio-Rad Laboratories Inc., Taiwan Branch (U.S.A.)
- 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
- Sep 13, 2017
- Expiry Date
- Sep 13, 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 "Burry" Spectrophotometer for Clinical Use (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number be4de7358252e2011dd1cd02f3f2510b and manufactured by BIO-RAD. The authorized representative in Taiwan is Bio-Rad Laboratories Inc., Taiwan Branch (U.S.A.).
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including BIO-RAD, 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.