Mindray AG 5 Agent Anesthetic Gas Analyzer Module V.1.0 Certified with Warranty
Mindray AG 5 Agent Anesthetic Gas Analyzer Module V.1.0 Certified with Warranty is backordered and will ship as soon as it is back in stock.
Couldn't load pickup availability
Mindray AG 5 Agent Anesthetic Gas Module V.1.0 6800-30-50502 Certified with a 90 Day Warranty
• Model: 6800-30-50502 (Mindray)
• Software Version: V.1.0
• Compatible with Passport 12m, Passport 17m, DPM 6+ and DPM 7+ Patient Monitors
• Weight: 4 lbs.
• Overall Length: 6 inches x 5 inches x 4 inches
The Mindray AG Module (Model 6800‑30‑50502, V.1.0) is a compact anesthetic gas analyzer module designed for real‑time monitoring of respiratory gases and volatile anesthetic agents. It employs sidestream sampling technology, which continuously draws a small gas sample (rather than being inline) to the sensor for measurement. This allows clinicians to monitor both expired (end‑tidal) and inspired gas concentrations of O₂, CO₂, N₂O, and a panel of five anesthetic vapors (Halothane, Enflurane, Isoflurane, Sevoflurane, Desflurane), with automatic agent identification and display of MAC (Minimum Alveolar Concentration) values. Such capability is especially valuable during surgeries under general anesthesia, procedural sedation, or in recovery settings, where knowing the depth of anesthetic and respiratory gas exchange is critical for patient safety.
Its physical design is made for integration: roughly 6″ by 5″ by 4″ and weighing about 4 lbs, the AG Module is intended to be plug‑and‑play with certain Mindray patient monitors. The interface allows for configuration of alarm thresholds, gas sampling rates or other settings (depending on monitor support), and includes sensors such as water traps to prevent condensation or moisture from interfering with measurement accuracy. The module includes failsafe features such as visual and audible alerts for sensor or hardware failures, low or high gas concentrations, water trap issues, or communication errors, ensuring that anomalies are quickly brought to clinician attention.
This medical equipment item has been certified by a service entity skilled or trained to work specifically on this type of device. The certification process may involve repair with replacement parts, calibration, and the periodic maintenance recommended by the original manufacturer. Additionally, cosmetic work and cleaning may have been performed to enhance the visual appeal of the equipment. This ensures that the equipment not only meets operational standards but also maintains a visually pleasing appearance.
No reviews available.
The Primis TeamProudly Supports
-
DAMIEN HOUSE
Located in Guayaquil, Ecuador, Damien House exists to provide care and help dispel the stigma of those affected by Hansen's Disease (Leprosy).
-
PROJECT PERFECT WORLD
Project Perfect World provides orthopedic surgery for children worldwide.






