Taiwan FDA registration 4df802a2a455c2c4e5831ac51e11c154
“Immucor” PanoscreenⅠ,Ⅱ and Ⅲ
TW: “依免可” 紅血球抗體篩選試劑
Taiwan·Risk Class 2·MD·IMMUCOR, INC.·Registered Oct 07, 2015 – Oct 07, 2025ExpiredRegistration details
- Analysis ID
- 4df802a2a455c2c4e5831ac51e11c154
- License Form
- Ministry of Health Medical Device Import No. 027709
- Customs Code
- DHA05602770907
Company information
- Manufacturer
- IMMUCOR, INC.
- Manufacturer Country
- United States
- Authorized Representative
- Y.H. BIOTEK CO., LTD.
Product details
- Intended Use
- Detection of unanticipated red blood cell antibodies.
- Product Type (Level 1)
- B Hematology and pathology devices
- Product Type (Level 2)
- B9650 Quality control equipment for blood bank reactors
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 07, 2015
- Expiry Date
- Oct 07, 2025
About this record
Access comprehensive regulatory information for “Immucor” PanoscreenⅠ,Ⅱ and Ⅲ in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4df802a2a455c2c4e5831ac51e11c154 and manufactured by IMMUCOR, INC.. The authorized representative in Taiwan is Y.H. BIOTEK CO., LTD..
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