Taiwan FDA registration 9b70f5ffee77e58dd5a0fa1bb76d8d4a

Jingming blood mixer for in vitro diagnostics

TW: 璟明體外診斷用血液混合器

Taiwan·Risk Class 1·Ruiming Instrument Co., Ltd·Registered Jul 10, 2009 – Jul 10, 2014Cancelled

Registration details

Analysis ID: 9b70f5ffee77e58dd5a0fa1bb76d8d4a

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 of identification scope of the Measures for the Administration of Medical Devices "Blood Mixers and Blood Gravimetric Analysis Devices (B.9195)".
Product Type (Level 1): B Hematology, pathology, and genetics
Product Type (Level 2): B.9195 Blood Mixers and Blood Gravimetric Analysis Devices
Import Information: Contract manufacturing;; Domestic

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 blood mixer for in vitro diagnostics in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9b70f5ffee77e58dd5a0fa1bb76d8d4a and manufactured by Ruiming Instrument Co., Ltd. The authorized representative in Taiwan is Jingming Industrial Co., Ltd.

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