SECTION 4 – TECHNICAL DATA
2022100-201 Rev C
© 2010 General Electric Company
Page 29 of 35
AED SELF-TEST SEQUENCE
Frequency of Self-Test
What is Tested?
Daily
Weekly
Monthly (every 28 days)
Open Lid (when lid is opened)
Close Lid (when lid is closed)
Battery, pads, internal electronics,
SHOCK/CONTINUE
button, and
software (no charge).
Battery, pads, internal electronics,
SHOCK/CONTINUE
button, and
software (partial charge).
Battery under load, pads, internal electronics, full-energy charge cycle,
SHOCK/CONTINUE
button, and software (full charge).
Battery, pads, internal electronics,
SHOCK/CONTINUE
button, and
software.
Battery, pads, internal electronics,
SHOCK/CONTINUE
button, and
software.
SAFETY AND PERFORMANCE STANDARDS
AED MODEL 2019198
The AED has been designed and manufactured to conform to the highest standards of safety and
performance including electromagnetic compatibility (EMC). The Responder AED Model 2019198 and pads
conform to the applicable requirements of the following:
CE
CE Marked by BSI 0086 per the Medical Device Directive 93/42/EEC of the
European Union
ETL
Classified by ETL Semko with respect to electric shock, fire and mechanical
hazards only in accordance with UL 60601-1, CAN/CSA C22.2 No.601.1-M90,
EN60601-1 and EN60601-2-4. Conforms to UL Standard UL60601-1. Certified
to CAN/CSA Standard C22.2 No. 601.1-M90.
Electrical, Construction, Safety and Performance
IEC 60601-1 (1998), Amendments 1 (1991) & 2 (1995)
IEC 60601-2-4 (2002)
IEC 60601-1-4 (2000)
ANSI/AAMI DF-39 (1993)
Electromagnetic Compatibility (EMC
)
IEC 60601-1-2 (2001)
IEC 60601-2-4 Section 36
ANSI/AAMI DF-39(1993) Section 3.3.21
The unit is safe for human use in compliance with the IEC 60601-1 Safety Analysis Tests standard.