Taiwan FDA registration 1748f3620e17433ae50c7bfede75a4e4
“Immucor” Anti-Jkb (Monoclonal) Gamma-clone
TW: “依免可” 單株抗體抗Jkb血型試劑
Taiwan·Risk Class 2·MD·IMMUCOR, INC.·Registered Jul 29, 2015 – Jul 29, 2025ExpiredRegistration details
- Analysis ID
- 1748f3620e17433ae50c7bfede75a4e4
- License Form
- Ministry of Health Medical Device Import No. 027539
- Customs Code
- DHA05602753908
Company information
- Manufacturer
- IMMUCOR, INC.
- Manufacturer Country
- United States
- Authorized Representative
- Y.H. BIOTEK CO., LTD.
Product details
- Intended Use
- It is suitable for the detection of red blood cell Jkb (Jk2) antigen in test by test in vitro test.
- 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
- Jul 29, 2015
- Expiry Date
- Jul 29, 2025
About this record
Access comprehensive regulatory information for “Immucor” Anti-Jkb (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 1748f3620e17433ae50c7bfede75a4e4 and manufactured by IMMUCOR, INC.. The authorized representative in Taiwan is Y.H. BIOTEK CO., LTD..
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