Taiwan FDA registration 28f41bafddcd2c30c5d4c7df1b7f4733
Reagent for Mitsubishi urea nitrogen determination
TW: 三菱尿素氮測定用試劑
Taiwan·Risk Class 2·MITSUBISHI KAGAKU IATRON. INC.·Registered Jul 04, 2006 – Jul 04, 2011CancelledRegistration details
- Analysis ID
- 28f41bafddcd2c30c5d4c7df1b7f4733
- Customs Code
- DHA00601718908
Company information
- Manufacturer
- MITSUBISHI KAGAKU IATRON. INC.
- Manufacturer Country
- Japan
- Authorized Representative
- Jingxiang Co., Ltd
Product details
- Intended Use
- Measure urea nitrogen in human serum, blood and urine.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1770 尿素氮試驗系統
- Import Information
- import
Dates and status
- Registration Date
- Jul 04, 2006
- Expiry Date
- Jul 04, 2011
- Cancellation Date
- Oct 30, 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 Mitsubishi urea nitrogen determination in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 28f41bafddcd2c30c5d4c7df1b7f4733 and manufactured by MITSUBISHI KAGAKU IATRON. INC.. The authorized representative in Taiwan is Jingxiang Co., Ltd.
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