Taiwan FDA registration 3fe502bab76c8c0af4e056ef79258564
“Immucor” corQC Test System
TW: “依免可”核心品管試驗系統
Taiwan·Risk Class 2·MD·IMMUCOR, INC.·Registered Oct 13, 2017 – Oct 13, 2027ActiveRegistration details
- Analysis ID
- 3fe502bab76c8c0af4e056ef79258564
- License Form
- Ministry of Health Medical Device Import No. 030072
- Customs Code
- DHA05603007209
Company information
- Manufacturer
- IMMUCOR, INC.
- Manufacturer Country
- United States
- Authorized Representative
- Y.H. BIOTEK CO., LTD.
Product details
- Intended Use
- Used for routine quality control evaluation of blood bank reagents.
- 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 13, 2017
- Expiry Date
- Oct 13, 2027
About this record
Access comprehensive regulatory information for “Immucor” corQC Test System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3fe502bab76c8c0af4e056ef79258564 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