2026116-001 Revision B Responder™ 2000 Page 19
SYMBOL DESCRIPTIONS
The following symbols may appear in this manual, on the Responder 2000, or on its accessories. Some of the symbols
represent standards and compliances associated with the Responder 2000 and its use.
Consult instructions for use of the Responder 2000 and/or its accessories.
Precaution: Consult accompanying documents
Authorized Representative in the European Community
CE Marked per the Medical Device Directive 93/42/EEC of the European Union. The
notified body is BSI (ID# 0086).
CE Mark: The Responder 2000 battery charger conforms to essential requirements of
Directive EMC 83/336/EEC.
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, IEC 60601-1 and IEC
60601-2-4. Conforms to UL Standard UL60601-1. Certified to CAN/CSA Standard C22.2
No. 601.1-M90.
Dangerous Voltage: The defibrillator output has high voltage and can present a shock
hazard. Please read and understand all safety alerts in this manual before attempting to
operate the Responder 2000.
xx/xxxx
Month and Year of manufacture.
Defibrillation-proof Type BF Applied Part = The SpO2 sensor/cable is isolated and can
withstand the effects of an externally applied defibrillation shock to the patient.
Defibrillation-proof Type CF Applied Part = The ECG, Pads, Paddles, and Spoon are
isolated, can withstand the effects of an externally applied defibrillation shock to the patient,
and are specifically designed for applications where a conductive connection directly to the
heart is established.
Device Model Number. Battery Model Number.
For use by or on the order of a Physician, or persons licensed by state law.
Lot Number
Manufacturer
Points to important information regarding the use of the Responder 2000.
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