Taiwan FDA registration c5280042d79036f5158898ec8257cd01
"Yikaifu" hemoglobin quality control control solution
TW: "易凱福" 血色素品管對照液
Taiwan·Risk Class 2·EKF-DIAGNOSTIC GMBH·Registered Feb 15, 2006 – Feb 15, 2016CancelledRegistration details
- Analysis ID
- c5280042d79036f5158898ec8257cd01
- Customs Code
- DHA00601599002
Company information
- Manufacturer
- EKF-DIAGNOSTIC GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- Y.H. BIOTEK CO., LTD.
Product details
- Intended Use
- The EKF Hemoglobin Control Solution is a quality control for periodic confirmation of the precision and accuracy of Hemo_Control photometer and microcomparator.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Import Information
- import
Dates and status
- Registration Date
- Feb 15, 2006
- Expiry Date
- Feb 15, 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 "Yikaifu" hemoglobin quality control control solution in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c5280042d79036f5158898ec8257cd01 and manufactured by EKF-DIAGNOSTIC GMBH. The authorized representative in Taiwan is Y.H. BIOTEK CO., LTD..
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