Taiwan FDA registration 5bf5c3ac481aa790565c0e1a5beacebc
“Immucor” Anti-Jka (Monoclonal) Gamma-clone
TW: “依免可” 抗Jka血型試劑(單株抗體)
Taiwan·Risk Class 2·MD·IMMUCOR, INC.·Registered Nov 03, 2015 – Nov 03, 2025ExpiredRegistration details
- Analysis ID
- 5bf5c3ac481aa790565c0e1a5beacebc
- License Form
- Ministry of Health Medical Device Import No. 027900
- Customs Code
- DHA05602790000
Company information
- Manufacturer
- IMMUCOR, INC.
- Manufacturer Country
- United States
- Authorized Representative
- Y.H. BIOTEK CO., LTD.
Product details
- Intended Use
- Suitable for the detection of red blood cell Jka (Jk1) antigen in IVF tests.
- Product Type (Level 1)
- B Hematology and pathology devices
- Product Type (Level 2)
- B4020 Analyze specific reagents
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Nov 03, 2015
- Expiry Date
- Nov 03, 2025
About this record
Access comprehensive regulatory information for “Immucor” Anti-Jka (Monoclonal) Gamma-clone in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5bf5c3ac481aa790565c0e1a5beacebc and manufactured by IMMUCOR, INC.. The authorized representative in Taiwan is Y.H. BIOTEK CO., LTD..
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