Heartsync by Vermed
GRAPHIC CONTROLS ACQUISITION CORP · Model PED-100
A noninvasive conductive material designed to facilitate electrical conduction between an external electrode (e.g., paddle-type defibrillator electrode) and the skin surface. It is available in various forms such as a thickened gel or polymer medium reinforced by a non-woven material, an adhesive pad/patch, or an absorbent material (e.g., felt) intended to be soaked in a conduction fluid. This is a single-use device.
Key tips
- ·Never skip the daily/shift ready-check - a defibrillator found dead during a code is a real, repeated root-cause finding.
- ·Pads and batteries have real expiration dates - check them on every PM, not just at annual service.
- ·Verify energy-delivery accuracy with a real defibrillator analyzer, not just a self-test pass.
PM Checklist
Preventive-maintenance tasks typical of this equipment class. Perform to the manufacturer's procedure and your facility's policy - this is general reference, not a schedule for this specific unit.
- ·Daily/shift visual and self-test check (AAMI EQ56 daily-ready standard)
- ·Battery and pad expiration-date tracking
- ·Energy-delivery accuracy test against a defibrillator analyzer
- ·Paddle/cable continuity check
- ·Annual full PM
Technical Specs
- Storage Environment Temperature
- 10°C to 40°C
- MRI safety
- Labeling does not contain MRI Safety Information
- Sterile
- No
- Single use
- Yes
- Prescription use
- Rx only
- FDA distribution status
- In Commercial Distribution
- Device type (GMDN)
- Electrode conductive skin pad, single-use
- FDA product classification
- Dc-Defibrillator, Low-Energy, (Including Paddles)
- Manufacturer support
- 800-669-6905 · info@vermed.com
Typical Location
Where this class of equipment is typically deployed - general reference, not this unit's own placement record.
- Crash carts (every unit)
- Emergency Department
- ICU
- OR
- Code-blue response areas
Documents & Manuals
No documents available for this device yet.
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