Taiwan FDA registration dec680a9cfcf76ca4c9ff9cadd33a8fe
“Immucor” Anti-K (Human Monoclonal) Series 2
TW: “依免可” 抗K血清(系列2)
Taiwan·Risk Class 2·MD·IMMUCOR, INC.·Registered Jan 16, 2014 – Jan 16, 2029ActiveRegistration details
- Analysis ID
- dec680a9cfcf76ca4c9ff9cadd33a8fe
- License Form
- Ministry of Health Medical Device Import No. 025857
- Customs Code
- DHA05602585702
Company information
- Manufacturer
- IMMUCOR, INC.
- Manufacturer Country
- United States
- Authorized Representative
- Y.H. BIOTEK CO., LTD.
Product details
- Intended Use
- This product is suitable for the detection of K antigen (kell or KEL1) by slide, test tube and microdisc method.
- Product Type (Level 1)
- B Hematology and pathology devices
- Product Type (Level 2)
- B9175 Automated Blood Sorting and Antibody Testing System
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jan 16, 2014
- Expiry Date
- Jan 16, 2029
About this record
Access comprehensive regulatory information for “Immucor” Anti-K (Human Monoclonal) Series 2 in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number dec680a9cfcf76ca4c9ff9cadd33a8fe and manufactured by IMMUCOR, INC.. 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