Thorpe Mill Pressure Care Cushion Foam - Inner for Sequential Cushion

Thorpe Mill Pressure Care Foam Cushion Inner

This Thorpe Mill pressure care foam cushion is the foam inner component designed for use within a sequential pressure care cushion system. It is supplied new and is intended for use in hospital bed, hospital trolley and patient trolley applications where pressure area management is a clinical requirement.

Checked Before Dispatch

This item is supplied new. Pre-dispatch checks include:

• Visual inspection for transit damage
• Verification against the store product record and barcode (GTIN: 5060026593639)

These are in-house checks only. A full engineer service is not applicable to a foam consumable. Commissioning and verification within a clinical system remain with the operating organisation.

Compatibility

This foam inner is designed as a replacement or spare component for a compatible sequential pressure care cushion. It is not a standalone pressure relief device. Check before ordering that the foam dimensions and specification match your existing sequential cushion assembly.

Clinical Context

Pressure care foam cushions are used as part of pressure area management protocols in ward, theatre and patient transport settings. The foam inner within a sequential cushion system provides the structural support layer beneath the sequential cell or cover component. High-density foam is commonly specified in these systems to maintain consistent support as cell pressure cycles.

Key Features

• New condition, supplied unused, suitable for direct integration into a clinical environment subject to local decontamination and commissioning protocols
• Compatible application, intended for hospital bed, hospital trolley and patient trolley use
• Inner component, forms part of a sequential cushion assembly and is not a complete pressure care system
• Manufacturer reference, THH1225A02 from Thorpe Mill, enabling straightforward identification against procurement records

Important Notes

This item is a consumable foam component. Its suitability for a specific patient must be determined by a competent clinician in accordance with local pressure care protocols and any relevant manufacturer instructions. The manufacturer instructions take precedence over any general guidance given here.

Information on this page is provided for guidance and does not replace advice from a qualified clinician. Always read the manufacturer's instructions before use, and check that a device is suitable for the patient and the prescribed therapy.