FDA product code QBP
Cap, Device Disinfectant
General Hospital·Class 2·21 CFR 880.5440
US regulatory classifications
- US Product Code (FDA)
- QBPView Product Code Classification →
- US Risk Class (FDA)
- Class 2
- US Regulation (CFR)
- 21 CFR 880.5440View CFR Regulation →
- Medical specialty
- General Hospital
Device characteristics
- GMP exempt
- No
- Implantable
- No
- Life-sustaining
- No
- Third party review
- Not Eligible
Definition
Disinfect needleless access valves and may act as a physical barrier to contamination if not removed for a set period of time
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About this record
Cap, Device Disinfectant is a medical device type in the General Hospital 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.