FDA product code NWY
Test, Qualitative, Detection Of Dengue Igm And Igg Antibodies
Unknown·Class N·21 CFR
US regulatory classifications
- US Product Code (FDA)
- NWYView Product Code Classification →
- US Risk Class (FDA)
- Class N
- US Regulation (CFR)
- 21 CFRView CFR Regulation →
- Medical specialty
- Unknown
Device characteristics
- GMP exempt
- No
- Implantable
- No
- Life-sustaining
- No
- Third party review
- Not Eligible
Definition
Intended for the detection of IgM and IgG antibodies to dengue virus in human serum, plasma or whole blood.
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About this record
Test, Qualitative, Detection Of Dengue Igm And Igg Antibodies is a medical device type in the Unknown specialty. This page includes real-world medical device registration data worldwide for this device type, with registrations from US FDA, Brazil ANVISA, and other global markets.
View regulatory classifications, recent 510(k) clearances, active device registrations, and similar products registered globally under this device category. Pure Global AI's free directory provides comprehensive worldwide registration intelligence across 7,000+ medical device types and 21 specialties.