Taiwan FDA registration 47175d1c6fbe447ac0aa29dae831f0d4
Dermanson Müster Myoglobin Flax Reagent Group
TW: 德曼遜敏斯特肌紅蛋白弗列克斯試劑組
Taiwan·Risk Class 2·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Registered Mar 16, 2012 – Mar 16, 2017CancelledRegistration details
- Analysis ID
- 47175d1c6fbe447ac0aa29dae831f0d4
- Customs Code
- DHA00602335409
Company information
- Manufacturer
- SIEMENS HEALTHCARE DIAGNOSTICS INC.
- Manufacturer Country
- United States
- Authorized Representative
- SIEMENS LIMITED
Product details
- Intended Use
- This product is equipped with the Dimension Vista system to measure the concentration of myoglobin in human serum and plasma.
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.5680 肌紅蛋白免疫試驗系統
- Import Information
- import
Dates and status
- Registration Date
- Mar 16, 2012
- Expiry Date
- Mar 16, 2017
- Cancellation Date
- Dec 13, 2019
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Dermanson Müster Myoglobin Flax Reagent Group in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 47175d1c6fbe447ac0aa29dae831f0d4 and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS INC.. The authorized representative in Taiwan is SIEMENS LIMITED.
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