FDA product code BTT
Humidifier, Respiratory Gas, (Direct Patient Interface)
Anesthesiology·Class 2·21 CFR 868.5450
US regulatory classifications
- US Product Code (FDA)
- BTTView Product Code Classification →
- US Risk Class (FDA)
- Class 2
- US Regulation (CFR)
- 21 CFR 868.5450View CFR Regulation →
- Medical specialty
- Anesthesiology
Device characteristics
- GMP exempt
- No
- Implantable
- No
- Life-sustaining
- No
- Third party review
- Not Eligible
Search keywords
Click to search for similar devices in our global database
About this record
Humidifier, Respiratory Gas, (Direct Patient Interface) is a medical device type in the Anesthesiology 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.