Philips M2636B Telemon Patient Monitor

Philips M2636B Telemon Patient Monitor

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Philips M2636B Telemon Patient Monitor at the lowest price. Please call for details.

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The Philips M2636B Telemon is indicated for use in the monitoring, recording, and alarming of multiple physiologic parameters in adult and pediatric patients to gain information for treatment, to monitor adequacy of treatment, or to exclude causes of symptoms. TeleMon is a prescription device for use in healthcare facilities by trained healthcare professionals. TeleMon is not intended for home use.



  1. ·          Maximum Pressure: 280 mmHg
  2. ·          Overpressure Safety Limit: 300 mmHg (max)
  3. ·          Accuracy: 5% of reading (whichever is greater)
  4. ·          Heart Rate Range: 40 to 200 b/min
  5. ·          Cuff Deflation Rate: 6 mmHg/step
  6. ·          NBP Alarm Range at Central: 10 to 260 mmHg
  7. ·          Rated Life: 30,000 measurement cycles (36/day for 2.3 years)
  8. ·          Cuff Inflation Time: 60 sec maximum
  9. ·          Limitations on Use: Not for use on neonates.
  10. ·          When used on patients suffering from cardiac arrhythmias, information presented will have undefined accuracy.
  11. ·          Auto Mode Repetition Time: 5, 10, 15, 30, 60 or 120 minutes
  12. ·          Measurement Time (average @ HR > 60 b/ min): Auto/Manual mode: 30 sec (average)
  13. ·        Auto/Manual mode: 170 sec (maximum)


Safety Standards

The M2636B TeleMon B Monitor complies with the Council Directive 93/42/EEC of 14 June, 1993 concerning medical devices, and carries CE marking accordingly (CE 0123).
The following accessories and system components are independently CEmarked:
Power Supply accessory Battery and Battery Reconditioner accessory

Telemetry System

Note—The Battery Reconditioner is not for use in the patient vicinity.

The M2636B TeleMon B also complies with the following international safety regulations for medical electrical equipment:
IEC 60601-1/ EN 60601-1
IEC 60601-1-1/ EN 60601-1-1
IEC 60601-1-2/ EN 60601-1-2
CAN/ CSA C22.2 No. 601.1-M90
UL 2601-1

This CISPR-11 Class A, Group 1 device is not suitable for use in a domestic establishment or one that is connected directly to the low voltage public mains. The monitor is a Class 1 device and has an IPX 1 rating (excluding the power supply). The device has BF and CF applied parts. The system provides continuous operation when in use.

Non-invasive blood pressure measurements determined with this device are equivalent to those obtained by a trained observer using the cuff/stethoscope auscultation method, within the limits prescribed by the American National Standard, Electronic or automated sphygmomanometers. Diastolic values correspond to Phase 5 Korotkoff sounds. The NPB portion of the device also meets all relevant parts of the following safety standards:
IEC 60601-2-30

NBP internal operating software ensures that:
Maximum cuff inflation time is limited to 60 seconds.
Duration of blood pressure reading is limited to 170 seconds.

Electrical Specifications

Line Power
Power Input An external power supply is used.
Input 100-250 VAC +6%/-10%; 50-60 Hz +/-6%
Input Power Average (36 Watts, 64 VA), Max (39 Watts, 81 VA)
Output 18 VDC
Battery Type 10.8V Nickel Metal Hydride Battery NI1030AG
(NiMH Smart Battery, package style DR 35), M4790A
Operating Time Typical 5 hours at 25º C (77º F) with %SpO2 and NBP measurements 4 times/hour: up to 3.5 hours
Charge Time From 15% of capacity to fully charged: 2-3 hours typical at 25º C (77º F), TeleMon on or off
Electrodes Compatible with EC-12 electrodes only

Environmental Specifications

Operating Temperature Range Monitor without NBP Cuff: 0º C to 35º C (32º F to 95º F)
Monitor with NBP Cuff: 10º C to 35º C (50º F to 95º F)
Altitude Range Up to 3048 m (10,000 ft.)
Humidity Range < 90% relative humidity at 35º C (95º F), noncondensing

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