Taiwan FDA registration be5c66487db8ec72f2d3226ff2375ee8
"Ikefu" hemoglobin microcolorimetric tablets
TW: "易凱福" 血色素微量比色片
Taiwan·Risk Class 2·EKF-DIAGNOSTIC GMBH·Registered Nov 11, 2005 – Nov 11, 2015CancelledRegistration details
- Analysis ID
- be5c66487db8ec72f2d3226ff2375ee8
- Customs Code
- DHA00601460201
Company information
- Manufacturer
- EKF-DIAGNOSTIC GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- Y.H. BIOTEK CO., LTD.
Product details
- Intended Use
- It is used to quantitatively determine the concentration of hemoglobin in human arterial, venous or microvascular blood.
- Product Type (Level 1)
- B Hematology, pathology, and genetics
- Product Type (Level 2)
- B.5620 Automated Heme Analysis System
- Import Information
- import
Dates and status
- Registration Date
- Nov 11, 2005
- Expiry Date
- Nov 11, 2015
- 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" hemoglobin microcolorimetric tablets in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number be5c66487db8ec72f2d3226ff2375ee8 and manufactured by EKF-DIAGNOSTIC GMBH. The authorized representative in Taiwan is Y.H. BIOTEK CO., LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices