Taiwan FDA registration 8ec05451ed3ca6843fe453e7d8cdb0dc
“Immucor” Anti-A series 1
TW: “依免可”抗A血清(系列1)
Taiwan·Risk Class 3·MD·IMMUCOR, INC.·Registered Aug 13, 2013 – Aug 13, 2028ActiveRegistration details
- Analysis ID
- 8ec05451ed3ca6843fe453e7d8cdb0dc
- License Form
- Ministry of Health Medical Device Import No. 025261
- Customs Code
- DHA05602526105
Company information
- Manufacturer
- IMMUCOR, INC.
- Manufacturer Country
- United States
- Authorized Representative
- Y.H. BIOTEK CO., LTD.
Product details
- Intended Use
- Identification of blood group A, suitable for slide, tube and microdisc testing.
- 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
- Aug 13, 2013
- Expiry Date
- Aug 13, 2028
About this record
Access comprehensive regulatory information for “Immucor” Anti-A series 1 in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 8ec05451ed3ca6843fe453e7d8cdb0dc and manufactured by IMMUCOR, INC.. The authorized representative in Taiwan is Y.H. BIOTEK CO., LTD..
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