Taiwan FDA registration ca735ed8d780eefcb1c3a21c0b50384d
Japanese photoelectric 3D hematology tube solution
TW: 日本光電3D血液學品管液
Taiwan·Risk Class 2·R&D SYSTEMS, INC.·Registered Dec 29, 2010 – Dec 29, 2015CancelledRegistration details
- Analysis ID
- ca735ed8d780eefcb1c3a21c0b50384d
- Customs Code
- DHA00602193101
Company information
- Manufacturer
- R&D SYSTEMS, INC.
- Manufacturer Country
- United States
- Authorized Representative
- Jingxiang Co., Ltd
Product details
- Intended Use
- This reagent contains 3 concentrations of quality tube fluids and is designed to monitor the performance of the Nihon Kohden Automated Hematology Analyzer.
- Product Type (Level 1)
- B Hematology, pathology, and genetics
- Product Type (Level 2)
- B.8625 Hematology Quality Control Mixtures
- Import Information
- import
Dates and status
- Registration Date
- Dec 29, 2010
- Expiry Date
- Dec 29, 2015
- Cancellation Date
- Jun 07, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Japanese photoelectric 3D hematology tube solution in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ca735ed8d780eefcb1c3a21c0b50384d and manufactured by R&D SYSTEMS, INC.. The authorized representative in Taiwan is Jingxiang Co., Ltd.
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