KPE · Class II · 21 CFR 880.5025

FDA Product Code KPE: Container, I.v.

Under FDA product code KPE, intravenous fluid containers are cleared for the storage and delivery of sterile IV solutions.

These flexible plastic bags or rigid bottles contain sterile isotonic, hypertonic, or hypotonic solutions — including saline, dextrose, and lactated Ringer's — for intravenous fluid and electrolyte replacement. They are a fundamental component of fluid therapy across all clinical settings.

KPE devices are Class II medical devices, regulated under 21 CFR 880.5025 and reviewed by the FDA General Hospital panel.

Leading manufacturers include Epic Medical Pte. , Ltd., Technoflex Sas. and Fresenius Kabi AG.

117
Total
117
Cleared
108d
Avg days
1976
Since
117 devices
49–72 of 117
No devices found for this product code.