Biolight Meditech S10 - Product Difference

S10/S12/S10A/S12A Patient Monitor User’s Manual
1-2
——with excessive and continuous patient movement such as shivering or
convulsions;
——if a regular arterial pressure pulse is hard to detect;
——with cardiac arrhythmias;
——with rapid blood pressure changes;
——with severe shock or hypothermia that reduces blood flow to the
peripheries;
——on a edematous extremity.
 RESP monitoring and apnea alarm based on chest impedance method are not
suitable for patients with obstructive sleep apnea.
 Patients with chronic septicemia or hypercoagulable state cannot consider
using this equipment. Because this equipment may cause suppurative or
non-irritating thrombus;
 Patients with Parkinson's disease and tricuspid valve prolapse may be at risk
of arrhythmia.
 C.O. measurement has limitations. C.O. measurement is not appropriate when
the patient meets one or more of the following conditions:
◆Low immune system
◆Right heart valve disease
◆Coagulopathy ◆Vascular disease
◆Thrombolytic therapy ◆Pulmonary hypertension
◆Pacemaker patient ◆Systemic hypotension
1.3. Product difference
Model
S12A S10A S12 S10
Displayscreen size 12.1 10.4 12.1 10.4
The number of NIBP
measurement result
≥4800 ≥4800 ≥2400 ≥2400
Functional differences
Support ECG, HR,
RR, TEMP, SpO2,
PR, NIBP, CO2,
IBP and C.O.
measurement
Support ECG,
HR, RR,
TEMP, SpO2,
PR and NIBP
measurement
Support ECG, HR,
RR, TEMP, SpO2,
PR, NIBP, CO2,
IBP and C.O.
measurement
Support ECG,
HR, RR, TEMP,
SpO2, PR and
NIBP
measurement