Current through Register Vol. 28, No. 7, January 1, 2025
Section 4303-10.0 - Defibrillation Equipment10.1 Defibrillators acceptable for use in the State of Delaware will: 10.1.2 Be of the semi-automatic type requiring provider intervention to initiate a defibrillation shock or other device as approved by the State EMS Medical Director.10.1.3 Be capable of automatically collecting data;10.1.4 Be capable of producing a printed summary report as approved by the State EMS Medical Director.10.1.5 SAED's utilizing alternate waveform technologies are approved for use provided that the treatment algorithm has been approved by the FDA.10.2 Defibrillation Equipment Modification 10.2.1 No modifications are to be made to defibrillation equipment, by a provider on the service, which results in: 10.2.1.1 Deviation from the original manufacturer's specification;10.2.1.2 Deviation from Early Defibrillation Program protocols.10.2.2 Defibrillation Protocol changes may only be authorized by the State EMS Medical Director.10.2.3 Necessary defibrillator modifications shall be coordinated by the Service Coordinator.10.2.4 Defibrillator preventive maintenance will be maintained in accordance with manufacturer's recommendations10.3 Financial Responsibility 10.3.1 Purchase of SAED units, electrodes or pads, data collection hardware/software and any required inspections, repairs or replacement parts shall be the sole responsibility of the service.16 Del. Admin. Code § 4303-10.0
17 DE Reg. 438( 10/1/2013) (Final)