Introduction
2067634-131 Revision E
SEER ™ 1000
17
ATTENTION
RECORDINGS OF LOSS OR INSUFFICIENT ECG SIGNAL QUALITY - It may be that
the recorder be used with unsatisfactory results if the patient does not have all the
necessary information.
It is the responsibility of the physician, give the patient the necessary information for an
evaluable ECG recording. In the section "
Inform the patient
evaluable ECG recording. In the section "
Inform the patient
evaluable ECG recording. In the section "
Inform the patient
ATTENTION
INTERFERENCE - electrical emissions of an electric blanket can reduce the signal quality.
Do not use the recorder with an electric blanket.
Medical Device Classification
The device is classified as follows, according to IEC 60601-1:
Medical Device Classification
Category
ranking
protection against electric shock Degree
Type CF, application component not protected
defibrillator
Protection against ingress of dust and
water
The recorder's protection class is IP43,
with:
4 = Protection against objects> 1 mm 3 =
Protection against splashing water
The level of security when used in the
presence of flammable mixtures and
anesthetic agents and oxygen or air or
nitrous oxide
The device is not suitable for use in the
presence of a flammable mixture of anesthetic
and air or oxygen or laughing gas.
sterilization and disinfection process
suggested by the manufacturer
Not applicable
operational
continuous operation
