Model note · Anaesthesia Machine
Mindray A-Series A7 Anesthesia System
The Mindray A7 is a continuous flow anaesthesia workstation with an automatic bellows ventilator and built in monitoring of O2, CO2, N2O and five anaesthetic agents. It is cleared for adults and all paediatric groups, neonates included. It belongs to Mindray's A-Series alongside the A3 and A5. FDA records show few recalls, mostly gas leaks at cylinder yokes and absorber seals across the A-Series.
The model
Maker, model and type.
- Maker
- Shenzhen Mindray Bio-Medical Electronics Co., Ltd. (Mindray)
- Model
- A7 Anesthesia System
- Device type
- Anaesthesia Machine
- Main document
- Open the public document
Key specifications
What the public record says.
| Item | Value | Source |
|---|---|---|
| FDA classification | Anaesthesia gas machine, 21 CFR 868.5160, Class II, product code BSZ, with secondary gas analyser and vacuum regulator codes | Source |
| Clearances | K142552 (2015), K151954 (2015), K171292 (decided 12 January 2018); A5/A7 update K253330 (2026) | Source |
| Vaporisers | Two or three variable bypass vaporisers; sevoflurane, isoflurane, desflurane, halothane and enflurane | Source |
| Ventilator | Automatic bellows ventilator, 1500 mL bellows; modes VCV, PCV, PCV-VG, SIMV-VC, SIMV-PC, PS | Source |
| Ventilation settings | Tidal volume 20 to 1500 mL; rate 4 to 100 bpm; I:E 4:1 to 1:8; inspiratory pause off or 5 to 60%; PEEP off or 3 to 30 cmH2O; pressure limit up to 100 cmH2O | Source |
| Fresh gas flow ranges | O2 and air 0 to 15 L/min, N2O 0 to 12 L/min; accuracy 50 mL/min or 5% of setting, whichever is greater | Source |
| Gas module sampling | Adult and paediatric 120, 150 or 200 mL/min; neonate 70, 90 or 120 mL/min; full accuracy about 10 minutes after start | Source |
| Other features | Heated breathing circuit, automatic system checks at start up, pressure volume and flow volume loops, Fresh Flow Optimizer, suction | Source |
Recalls
Known FDA recalls.
- Z-2689-20162016-06-15
Possible leak at the backup O2 and air E size cylinder yokes.
FDA record
Safety
Safety warnings from the record.
Sources
Where this note comes from.
- FDA 510(k) K171292 summary, A7 Anesthesia System
- openFDA recall search, Mindray A-Series anaesthesia
- openFDA MAUDE problem counts, brand A7 Anesthesia System
Not covered: No Mindray product page or manual was opened, so manufacturerUrl points to the FDA summary and errorCodes is empty. The 510(k) comparison table extracted out of order; values were matched to rows by position and should be checked against the PDF. Battery, gas supply pressure, weight and electrical data were not found. The A3/A5 recalls are a related product line and are used only as guidance, not as A7 recalls. Recall text was read through openFDA because FDA recall pages returned errors at drafting time.
BMEssentia knowledge drafted from public information, reviewed by Hasan Khaled Ismail on 2026-10-24. Always follow the manufacturer's instructions for use and service manual.
Anaesthesia Machine
Other models of this device.
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