Taiwan FDA registration d8223fb365ceedf81a7057a7da94866d
Innova rheumatoid factor immunoglobulin A chemical cold light immunoassay reaction reagent
TW: 因諾瓦類風濕因子免疫球蛋白A化學冷光免疫分析法反應試劑
Registration details
- Analysis ID
- d8223fb365ceedf81a7057a7da94866d
- Customs Code
- DHA05603329607
Company information
- Manufacturer
- INOVA Diagnostics, Inc
- Manufacturer Country
- United States
- Authorized Representative
- TRUGENE DIAGNOSTICS, INC.
Product details
- Intended Use
- This product uses chemical cold light immunoassay to semi-quantify anti-rheumatoid factor immunoglobulin A antibodies in human serum samples.
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.5775 類風濕性因子免疫試驗系統
- Import Information
- Input;; QMS/QSD
Dates and status
- Registration Date
- Mar 17, 2020
- Expiry Date
- Mar 17, 2025
About this record
Access comprehensive regulatory information for Innova rheumatoid factor immunoglobulin A chemical cold light immunoassay reaction reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d8223fb365ceedf81a7057a7da94866d 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