Secondhand Philips HeartStart HS1 AED Defibrillator

Objective AI Report

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Report date: 08.12.2025

Philips HeartStart HS1 Defibrillator Device Analysis Report

Device Identification

The product shown in the images is an Automated External Defibrillator (AED) device, a portable medical device that delivers an electrical shock to restore the heart’s normal rhythm in cases of sudden cardiac arrest. The device is seen as a complete set, including its protective carrying case and accompanying consumables.

Brand and Model

The device’s front panel, rear label, and logos on the carrying case have been thoroughly examined. As a result of the analysis:

• Brand: Philips
• Model: HeartStart HS1 (Clearly indicated as “HEARTSTART HS1” on the label and “HeartStart Home Defibrillator” on the front).

Authenticity

Upon examining the Philips logos, “HeartStart” branding, placement of warning labels, original technical labels containing REF and SN codes (Philips Medical Systems), the device’s molding quality, and international standard symbols (CE, CSA, IP21), the product has been determined to be Original. The case and accessories are also original Philips branded.

Areas of Use

This device is designed for emergency intervention for patients experiencing sudden cardiac arrest. As implied by the “Home Defibrillator” label, it is an easy-to-use, life-saving equipment equipped with audio and visual prompts, allowing use by individuals without medical training in homes, workplaces, or public areas. It is suitable for use on adults and, with appropriate pads, on children.

Quantity Information

The parts identified within the set in the images are as follows:

• 1 unit Philips HeartStart HS1 Defibrillator main unit.
• 1 unit M5070A Battery (Installed in the device).
• 1 unit Smart Electrode Pad Cartridge (Installed in the device).
• 1 unit Red HeartStart carrying case.
• 1 unit Response kit (Contains blue-handled scissors and likely a razor/gloves etc. in a black pouch).
• 1 unit Document and CD set (Quick Start guide, Turkish user manual, and CD).

General Condition

The device’s outer casing appears clean and is observed to be in good cosmetic condition. There is no significant yellowing or excessive wear on the device’s plastic surfaces. However, upon reviewing the dates of the consumables (pads and battery), it is understood that these parts have reached the end of their service life. This indicates that the device, in its current state, is “Not Ready for Use” and requires maintenance and part replacement.

Physical Deformation

No cracks, breaks, deep scratches, or dents have been detected on the device’s blue outer casing, keypad, or electrode slot. The red carrying case is intact, with no tears or rips observed.

Mechanical Components

The battery compartment cover and the mechanical latches of the electrode cartridge (green pull tab) appear robust. The case zipper and the condition of the internal elastic straps are satisfactory.

Electronic Components

The device features three main buttons (Green Power, Blue Info ‘i’, Orange Shock) and various indicator lights. There is no fading or deformation on the buttons. The electronic functionality could not be tested as the device was not powered on, but its physical integrity is complete.

Accessories

The device comes with a special red zippered carrying case (hard case/semi-hard case). An emergency response shears (for cutting clothes) is located in the inner compartment of the case. Additionally, a CD named “Power to save a life,” documents containing Turkish usage information (“TÜRKÇE: Philips, cihazın…” phrase is readable), and quick start cards are present.

Battery Status

The battery unit installed at the rear of the device has been examined in detail:

• Type: LiMnO2 (Lithium Manganese Dioxide), 9V DC, 4.2 Ah.
• Status: The label on the battery states “Install before 2021-09.” As this date has passed, the battery has likely reached the end of its life or is near depletion. It must be replaced or its charge level checked.

Label Information

The following technical data has been collected from the labels on the device and its parts:

• Device Model (REF): M5068A
• Serial Number (SN): A15K-05402
• Battery Part No (REF): M5070A (Also has code 62785P on it).
• Barcode: (01)00884838049130(21)A15K-05402
• Manufacturer’s Address: Philips Medical Systems, Bothell, WA 98021 USA.
• Certifications: CE 0123, CSA US, IP21 (Protection class).
• Notes: Batteries manufactured in the USA, assembled in Mexico.

Size and Compatibility

The pad cartridge bears the inscription “55+ lbs / 25+ kg.” This indicates that the pads installed in the device are suitable for patients weighing over 25 kg (adults). A separate pediatric pad cartridge (such as M5072A) is required for children/infants, but this pediatric pad is not present in the images.

Consumable Date Analysis (Manufacturing/Expiration)

The most critical details in the images are the dates on the consumables:

• Electrode Pads (Cartridge): The date “04/2018” is next to an hourglass icon. The expiration date for these pads has passed in April 2018. These pads should not be used as their gels may have dried out, and they must be replaced with new ones.
• Battery: The last installation date is stated as “2021-09.” Its shelf life has passed.
• Lot Number (Pad): Y072915-07

Documents

The set includes a Quick Start Guide, a document containing Turkish usage notes, and a CD. However, an invoice or warranty certificate was not seen in the images. The device’s warranty can be checked using its SN, but given its year of manufacture, it is highly probable that the warranty has expired.

Potential Malfunction Risk and Warnings

No signs of mechanical malfunction (such as cracks, breaks, oxidation, etc.) belonging to the device are present in the images. However, the product is a critical device used for life-saving purposes. Important Risk Warning: The electrode pads (EXP: 2018) and battery (Install: 2021) have passed their expiration/installation dates. In its current state, there is a risk of it not operating or not providing sufficient conductivity in an emergency. For the device to be put into active use, a new-dated battery and a new electrode pad cartridge must be purchased.