Taiwan FDA registration 9ea66b7f6b1f77b574f734a4833c0e56
Reagent for the determination of component C3 for Mitsubishi complement
TW: 三菱補體用成分C3測定用試劑
Taiwan·Risk Class 2·MITSUBISHI KAGAKU IATRON. INC.·Registered Jul 19, 2006 – Jul 19, 2011CancelledRegistration details
- Analysis ID
- 9ea66b7f6b1f77b574f734a4833c0e56
- Customs Code
- DHA00601722805
Company information
- Manufacturer
- MITSUBISHI KAGAKU IATRON. INC.
- Manufacturer Country
- Japan
- Authorized Representative
- Jingxiang Co., Ltd
Product details
- Intended Use
- The haze of supplement 3 (C3) in serum was analyzed.
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.5240 補體成份免疫試驗系統
- Import Information
- import
Dates and status
- Registration Date
- Jul 19, 2006
- Expiry Date
- Jul 19, 2011
- Cancellation Date
- May 23, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Reagent for the determination of component C3 for Mitsubishi complement in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9ea66b7f6b1f77b574f734a4833c0e56 and manufactured by MITSUBISHI KAGAKU IATRON. INC.. The authorized representative in Taiwan is Jingxiang Co., Ltd.
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