Taiwan FDA registration ac19b147f40d5d7bddbe06456cbfc8fd
Reagent for Mitsubishi immunoglobulin E assay
TW: 三菱免疫球蛋白E測定用試劑
Taiwan·Risk Class 2·MITSUBISHI CHEMICAL MEDIENCE CORPORATION PRODUCT AND LOGISTICS CENTER·Registered Jul 19, 2006 – Jul 19, 2016CancelledRegistration details
- Analysis ID
- ac19b147f40d5d7bddbe06456cbfc8fd
- Customs Code
- DHA00601723301
Company information
- Manufacturer Country
- Japan
- Authorized Representative
- Jingxiang Co., Ltd
Product details
- Intended Use
- The serum levels of non-specific IgE were analyzed.
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.5510 免疫球蛋白A,G,M,D及E免疫試驗系統
- Import Information
- import
Dates and status
- Registration Date
- Jul 19, 2006
- Expiry Date
- Jul 19, 2016
- 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 Reagent for Mitsubishi immunoglobulin E assay in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ac19b147f40d5d7bddbe06456cbfc8fd and manufactured by MITSUBISHI CHEMICAL MEDIENCE CORPORATION PRODUCT AND LOGISTICS CENTER. The authorized representative in Taiwan is Jingxiang Co., Ltd.
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