Taiwan FDA registration 1c281b3821623ed200ebc8b9862a704d
“Immucor” corQC EXTEND
TW: “依免可” 核心擴展品管血球試劑
Taiwan·Risk Class 2·MD·IMMUCOR, INC.·Registered Oct 24, 2017 – Oct 24, 2027ActiveRegistration details
- Analysis ID
- 1c281b3821623ed200ebc8b9862a704d
- License Form
- Ministry of Health Medical Device Import No. 030086
- Customs Code
- DHA05603008607
Company information
- Manufacturer
- IMMUCOR, INC.
- Manufacturer Country
- United States
- Authorized Representative
- Y.H. BIOTEK CO., LTD.
Product details
- Intended Use
- For manual and automated analysis (e.g. Galileo) Rh, Kell blood typing reagent quality control.
- 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 24, 2017
- Expiry Date
- Oct 24, 2027
About this record
Access comprehensive regulatory information for “Immucor” corQC EXTEND in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1c281b3821623ed200ebc8b9862a704d 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