Mapleson A circuit with 2.0 L reservoir bag, 1.6 m corrugated tubing and APL valve

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Mapleson A circuit with 2.0 L reservoir bag, 1.6 m corrugated tubing and APL valve Mapleson A circuit with 2.0 L reservoir bag, 1.6 m corrugated tubing and APL valve

Mapleson A Circuit

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Product Description

This Mapleson A circuit, also known as the Magill attachment, is a breathing system for adult anesthesia. A 2.0 L reservoir bag is mounted at the machine end with an APL valve, and a 1.6 m corrugated tube carries gas to the patient. The arrangement makes the circuit efficient for spontaneous ventilation, because fresh gas is not wasted during expiration.

Mapleson A is the most efficient of the Mapleson circuits for spontaneous ventilation. Because the reservoir bag and the APL valve sit at the machine end and the corrugated tube runs to the patient, the fresh gas that enters during expiration is stored and used for the next breath rather than being lost. In practice this means a lower fresh gas flow is needed than with Mapleson D or F during spontaneous breathing.

The same arrangement makes Mapleson A less suitable for controlled ventilation, where a much higher fresh gas flow is required to prevent rebreathing. Where controlled ventilation is needed, a Bain circuit (Mapleson D) is normally used instead.

Mapleson A circuit with 2.0 L reservoir bag, 1.6 m corrugated tubing and APL valve

Key Features:

  • Mapleson A (Magill attachment) configuration

  • 2.0 L reservoir bag

  • 1.6 m corrugated tubing with 22 mm internal diameter

  • APL valve for pressure relief

  • 30M and 22F connectors

  • Efficient for spontaneous ventilation

Applications:

  • Spontaneous ventilation in adult anesthesia

  • Where a Magill attachment system is specified

  • Low fresh gas flow spontaneous breathing

  • Adult patients

Important Notes:

  • Mapleson A is efficient for spontaneous ventilation but requires a high fresh gas flow during controlled ventilation.

  • Check the APL valve setting before use.

  • Check that the reservoir bag is correctly seated and is not twisted.

  • Confirm the connector size matches the airway device and the anesthesia machine.

  • Do not use if the package is damaged or opened.

  • Single use only unless the circuit is specified as reusable.

  • This product is a breathing system. It requires an anesthesia machine and trained personnel.

This product is manufactured under an ISO 13485:2016 certified quality management system (Certificate No. CN25-10207H) and is covered by Verification of Conformity No. ICR/VC/HM2603270. It is included in our FDA device listing, Owner/Operator No. 10096597.

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