FDA product code NZD
Stretcher, Patient Restraint
General Hospital·Class 1·21 CFR 880.6900
US regulatory classifications
- US Product Code (FDA)
- NZDView Product Code Classification →
- US Risk Class (FDA)
- Class 1
- US Regulation (CFR)
- 21 CFR 880.6900View CFR Regulation →
- Medical specialty
- General Hospital
Device characteristics
- GMP exempt
- Yes
- Implantable
- No
- Life-sustaining
- No
- Third party review
- Not Eligible
Definition
Soft restraints to be attached to a backboard or stretcher in order to immobilize the patient in emgency situations.
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About this record
Stretcher, Patient Restraint 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.