Taiwan FDA registration 1c8fa684871cf3aa195eefe7104796f4
Mitsubishi fully automated latex immunoassay system diluent
TW: 三菱全自動乳膠免疫分析系統稀釋液
Taiwan·Risk Class 1·MITSUBISHI CHEMICAL MEDIENCE CORPORATION YACHIYO AREA·Registered Nov 22, 2007 – Nov 22, 2012CancelledRegistration details
- Analysis ID
- 1c8fa684871cf3aa195eefe7104796f4
- Customs Code
- DHA04400631407
Company information
- Manufacturer Country
- Japan
- Authorized Representative
- Jingxiang Co., Ltd
Product details
- Intended Use
- Limited to the first level identification scope of "General Purpose Reaction Reagents (B.4010)" under the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- B Hematology, pathology, and genetics
- Product Type (Level 2)
- B.4010 Reaction Reagents for General Purposes
- Import Information
- import
Dates and status
- Registration Date
- Nov 22, 2007
- Expiry Date
- Nov 22, 2012
- Cancellation Date
- May 05, 2014
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Mitsubishi fully automated latex immunoassay system diluent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 1c8fa684871cf3aa195eefe7104796f4 and manufactured by MITSUBISHI CHEMICAL MEDIENCE CORPORATION YACHIYO AREA. The authorized representative in Taiwan is Jingxiang Co., Ltd.
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