Taiwan FDA registration 24bdf74369eb5e55d5f4039768e0f11f
"Borhenium" fluorescence analyzer (unsterilized)
TW: “博錸”螢光分析儀 (未滅菌)
Taiwan·Risk Class 1·PLEXBIO CO., LTD.·Registered Aug 08, 2013 – Aug 08, 2018CancelledRegistration details
- Analysis ID
- 24bdf74369eb5e55d5f4039768e0f11f
Company information
- Manufacturer
- PLEXBIO CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- PLEXBIO CO., LTD.
Product details
- Intended Use
- Limited to the first-level identification range of the Measures for the Administration of Medical Devices "Fluorescence Instrument for Clinical Use (A.2560)".
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.2560 Fluorometer for clinical use
- Import Information
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- Aug 08, 2013
- Expiry Date
- Aug 08, 2018
- Cancellation Date
- Jun 22, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Borhenium" fluorescence 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 24bdf74369eb5e55d5f4039768e0f11f and manufactured by PLEXBIO CO., LTD.. The authorized representative in Taiwan is PLEXBIO CO., LTD..
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