Taiwan FDA registration 4dd73e529903d1e70472d3684e6c2e3b
GB Troponin I EIA Kit
TW: 普生肌鈣蛋白I酵素免疫分析套組
Taiwan·Risk Class 2·MD·BIOCHECK, INC.·Registered Sep 24, 2015 – Sep 24, 2025ExpiredRegistration details
- Analysis ID
- 4dd73e529903d1e70472d3684e6c2e3b
- License Form
- Ministry of Health Medical Device Import No. 027692
- Customs Code
- DHA05602769203
Company information
- Manufacturer
- BIOCHECK, INC.
- Manufacturer Country
- United States
- Authorized Representative
- GENERAL BIOLOGICALS CORP.
Product details
- Intended Use
- Quantitatively determine the concentration of human serum central troponin I (cTnI).
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A1215 Creatine phosphocatalyzed?/creatine excitation or isomeric test system
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Sep 24, 2015
- Expiry Date
- Sep 24, 2025
About this record
Access comprehensive regulatory information for GB Troponin I EIA Kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4dd73e529903d1e70472d3684e6c2e3b and manufactured by BIOCHECK, INC.. The authorized representative in Taiwan is GENERAL BIOLOGICALS CORP..
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