Taiwan FDA registration 759dc18fa5005337a8b42446eb968235
"Ikefu" rapid hemoglobin correction control assay set group
TW: "易凱福" 快速血色素校正對照測定片設定組
Taiwan·Risk Class 2·EKF-DIAGNOSTIC GMBH·Registered Apr 11, 2006 – Apr 11, 2016CancelledRegistration details
- Analysis ID
- 759dc18fa5005337a8b42446eb968235
- Customs Code
- DHA00601633106
Company information
- Manufacturer
- EKF-DIAGNOSTIC GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- Y.H. BIOTEK CO., LTD.
Product details
- Intended Use
- 在使用Hemo_Control光度計和新測定之前,用以測定目標數值.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1660 Quality control materials (analytical and non-analytical)
- Import Information
- import
Dates and status
- Registration Date
- Apr 11, 2006
- Expiry Date
- Apr 11, 2016
- Cancellation Date
- Jun 28, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Ikefu" rapid hemoglobin correction control assay set group in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 759dc18fa5005337a8b42446eb968235 and manufactured by EKF-DIAGNOSTIC GMBH. The authorized representative in Taiwan is Y.H. BIOTEK CO., LTD..
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