Taiwan FDA registration 7a47765fa2860d0b330c0cab566beae6
QUANTA Flash RNP Controls
TW: 因諾瓦RNP化學冷光免疫分析法對照組
Taiwan·Risk Class 2·MD·INOVA DIAGNOSTICS, INC.·Registered Feb 16, 2015 – Feb 16, 2025ExpiredRegistration details
- Analysis ID
- 7a47765fa2860d0b330c0cab566beae6
- License Form
- Ministry of Health Medical Device Import No. 027079
- Customs Code
- DHA05602707900
Company information
- Manufacturer
- INOVA DIAGNOSTICS, INC.
- Manufacturer Country
- United States
- Authorized Representative
- TRUGENE DIAGNOSTICS, INC.
Product details
- Intended Use
- This product is used as a quality control control for QUANTA Flash RNP chemical cold light immunoassay.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A1660 Quality Control Materials (Analytical and Non-Analytical)
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Feb 16, 2015
- Expiry Date
- Feb 16, 2025
About this record
Access comprehensive regulatory information for QUANTA Flash RNP Controls in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7a47765fa2860d0b330c0cab566beae6 and manufactured by INOVA DIAGNOSTICS, INC.. The authorized representative in Taiwan is TRUGENE DIAGNOSTICS, INC..
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