FDA product code QGX

General Use Pneumatic Tourniquet

General, Plastic Surgery·Class 1·21 CFR 878.5910
US regulatory classifications
US Product Code (FDA)
QGX
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US Risk Class (FDA)
Class 1
US Regulation (CFR)
21 CFR 878.5910
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Medical specialty
General, Plastic Surgery
Device characteristics
GMP exempt
No
Implantable
No
Life-sustaining
No
Third party review
Not Eligible
Definition

A pneumatic tourniquet is an air-powered device consisting of a pressure-regulating unit, connecting tubing, and an inflatable cuff. The cuff is intended to be wrapped around a patient's limb and inflated to reduce or totally occlude circulation.

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About this record

General Use Pneumatic Tourniquet is a medical device type in the General, Plastic Surgery 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.