Philips Heartstart M3713A Multifunction FR2 /FR2+/FR3 Adult/Child Pad Cartridge
(10kg+) AED Expires 2027

Condition

New, sealed medical consumable in original packaging (unless otherwise stated).

Please review all photographs and verify the expiry date before purchase. Packaging may show minor storage wear.


Product Description

Genuine Philips HeartStart Multifunction Defibrillation Electrode Pads designed for compatibility with selected Philips HeartStart AED and defibrillator systems.

Suitable for use with adult and paediatric patients weighing over 10kg when used in accordance with the manufacturer's instructions for use (IFU).

Ideal replacement electrodes for maintaining operational readiness of compatible emergency response equipment.


Compatibility

Compatible with:

Please confirm compatibility with your device before purchasing.


Features


Included


Medical Device Information

This item is a medical device accessory intended for use in accordance with the manufacturer's instructions and applicable healthcare guidelines.

Purchasers are responsible for ensuring compatibility, suitability, installation, maintenance requirements and compliance with all local regulations.

This listing does not provide medical advice and does not make any claims regarding clinical outcomes or treatment effectiveness.


Shipping

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VAT

✓ 20% VAT Included in Sale Price

✓ VAT Invoice Available Upon Request


Returns

✓ 30 Days Free Returns

Please ensure sealed consumable items remain unopened if being returned.


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Important Information

Where applicable, purchasers should inspect packaging integrity and expiry information before use.

All trademarks, brand names and model references are used solely to identify compatibility and remain the property of their respective owners.

Please contact us with any compatibility questions before purchasing.

Users must read and follow all manufacturer instructions, warnings, and guidelines provided with the specific device and its accessories. It is recommended that the use of  pads and the associated stimulation settings be supervised or prescribed by a licensed healthcare provider to ensure suitability for an individual's health status.