Taiwan FDA registration 7fb107bb4a50efb3a3f4344fc956f1f6
Jingming in vitro diagnostic blood bank centrifuge
TW: 璟明體外診斷用血庫離心機
Taiwan·Risk Class 1·Ruiming Instrument Co., Ltd·Registered Jul 10, 2009 – Jul 10, 2014CancelledRegistration details
- Analysis ID
- 7fb107bb4a50efb3a3f4344fc956f1f6
Company information
- Manufacturer
- Ruiming Instrument Co., Ltd
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Jingming Industrial Co., Ltd
Product details
- Intended Use
- Limited to the first level identification range of blood bank centrifuge (B.9275) for in vitro diagnostic of medical equipment management methods.
- Product Type (Level 1)
- B Hematology, pathology, and genetics
- Product Type (Level 2)
- B.9275 Blood bank centrifuge for in vitro diagnostics
- Import Information
- Domestic;; Contract manufacturing
Dates and status
- Registration Date
- Jul 10, 2009
- Expiry Date
- Jul 10, 2014
- Cancellation Date
- Aug 09, 2018
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for Jingming in vitro diagnostic blood bank centrifuge in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 7fb107bb4a50efb3a3f4344fc956f1f6 and manufactured by Ruiming Instrument Co., Ltd. The authorized representative in Taiwan is Jingming Industrial Co., Ltd.
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