Product Manual

F6 and F6 Express Fetal & Maternal Monitor User Manual Safety Guide
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1.2 Features
The following table lists the measurements that F6 and F6 Express support.
Model
Measurement
F6
F6 Express
Dual-FHR √ √
TOCO √ √
FM √ √
AFM √ √
DECG/IUP Opt ×
MECG × √
NIBP × √
MSpO2 × √
TEMP × √
NOTE: √ = Standard Opt = Optional × = Not Available
1.3 Instruction for Safe Operation
NOTE:
In this manual, Monitor refers to both F6 and F6 Express, and is used where the
information applies to both models.
 The monitor is designed to comply with the international safety requirements IEC/EN
60601-1 for medical electrical equipment. It is class I equipment.
 The monitor operates within specifications at ambient temperatures between +5ºC (+41ºF)
and +40ºC (+104ºF). Ambient temperatures that exceed these limits could affect the
accuracy of the instrument and cause damage to the modules and circuits. Allow at least 2
inches (5 cm) clearance around the instrument for proper air circulation.
 You must check that the equipment, cables and transducers do not have visible evidence of
damage that may affect patient safety or monitoring capability before use. If damage is
evident, replacement is recommended before use.
 The monitor must be serviced only by authorized and qualified personnel. The manufacturer
does not accept responsibility for safety compliance, reliability and performance if
modifications or repairs are carried out by unauthorized personnel. Identical replacement
parts must be used.
 The protective categories against electric shock of the patient connections are: