Preconnected adult defibrillation electrodes for Medtronic, Mindray, Lecor and Bexen equipment. 1 pair

Preconnected single-use electrode pair indicated for defibrillation procedures, synchronized cardioversion, and electrocardiogram monitoring in adult patients. Manufactured with biocompatible materials and designed to be comfortable to place on the patient and withstand up to 15 discharges at 360 joules sequentially without damage.

General Features
- Electrodes compatible with defibrillation procedures, synchronized cardioversion, and ECG monitoring
- Provided with the connection cable outside the bag to keep them preconnected, ideal for emergency cases
- Able to withstand up to 15 discharges at 360 J consecutively
- Free of natural latex, phthalates and biologically sourced compounds
- Non-cytotoxic, non-sensitizing and non-irritating

Technical Specifications
- Electrode dimensions: 105 x 155 mm
- Active area dimensions: 79.45 cm2
- Recommended usage time: 24 h
- Minimum patient weight: 10 kg
- Shelf life: 2 years from the date of manufacture
- Compatibility: Physio-Control/Medtronic equipment (Lifepack 12, Lifepack 20e, and Lifepack 1000), Mindray (Beneheart D3), Lecor (Cor-Res A6S) and Bexen (Reanibex 200)

Materials
- Support: 1 millimeter thick white polyethylene foam with waterproof cell and biocompatible acrylic adhesive
- Conductive area: tin foil with biocompatible acrylic-based hydrogel
- Protector: polyethylene terephthalate
- Connection cable: copper (65/0.127 mm) coated with non-toxic polyvinyl chloride
- Connector mold: plastic material
- Ring terminals: brass
- Washer: ethylene vinyl acetate/thermoplastic elastomer

Electrical Properties
- Low frequency AC impedance at 10 Hz: < 3000 Ω
- Low frequency AC impedance at 30 kHz: < 10 Ω
- High frequency AC impedance: < 5 Ω
- Defibrillation overload recovery after 4 s: < 500 mV
- Defibrillation overload recovery after 60 s: < 400 mV
- DC Offset Voltage: < 100 mV

Standards and Certifications
- IEC 60601-2-4
- ISO 10993-5
- ISO 10993-10
- ISO 13485
- RoHS regulation
- Directive 93/42/EEC, class I medical device