Philips M5066A owner manual Separation distance according to frequency of transmitter m

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PHILIPS MEDICAL SYSTEMS

RECOMMENDED SEPARATION DISTANCES BETWEEN PORTABLE

AND MOBILE RF COMMUNICATIONS EQUIPMENT AND THE ONSITE

The OnSite is intended for use in an electromagnetic environment in which radiated RF disturbances are controlled. The customer or the user of the OnSite can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile RF communications equipment (transmitters) and the OnSite as recommended below, according to the maximum output power of the communications equipment.

 

separation distance according to frequency of transmitter (m)

 

rated maximum output

80 MHz to

800 MHz to

 

power of transmitter (W)

800 MHz

2.5 GHz

 

 

d = 0.6P

d = 1.15P

 

 

 

 

 

0.01

0.06

0.115

 

0.1

0.19

0.36

 

1

0.6

1.15

 

10

1.9

3.64

E

100

6.0

11.5

 

 

 

 

 

For transmitters rated at a maximum output power not listed above, the recommended separation distance d in meters (m) can be determined using the equation applicable to the frequency of the transmitter, where P is the maximum output power rating of the transmitter in watts (W) according to the transmitter manufacturer.

NOTE 1. At 80 MHz and 800 MHz, the separation distance for the higher frequency range applies.

NOTE 2. The ISM (industrial, scientific and medial) bands between 150 kHz and 80 MHz are 6,765 MHz to 6,795 MHz; 13,553 MHz to 13,567 MHz; 26,957 MHz to 27,283 MHz; and 40,66 MHz to 40,70 MHz.

NOTE 3. An additional factor of 10/3 is used in calculating the recommended separation distance for transmitters in the ISM frequency bands between 150 kHz and 80 MHz and in the frequency range 80 MHz to

2.5GHz to decrease the likelihood that mobile/portable communications equipment could cause interference if it is inadvertently brought into patient areas.

NOTE 4. These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection from structures, objects and people.

H-3

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Contents Edition A r t S t a r t O n S i t e D e f i b r i l l a t o rIntentionally blank Chirps HeartStartIntentionally blank Quick Reference Intentionally blank Important Note HeartStart OnSiteIntentionally blank Philips Medical Systems, Seattle, WA, USA Philips Electronics North America CorpIntentionally blank Contents Appendices Indications for USE Introduction to the HeartstartDescription Sudden Cardiac ArrestTraining and Practice National and Local RequirementsFor More Information Package Contents Setting UP the Heartstart OnsiteTop Back Philips Medical Systems Recommended Accessories Overview Using the Heartstart OnsitePull the Green Handle Place the Pads Patient, and the Caution light begins flashing as a reminder Press the Shock ButtonRemove the Infant/Child Pads Cartridge from its package Treating Infants and ChildrenDo not Delay Treatment When Emergency Medical Services ArriveReminders Philips Medical Systems Must be replaced after being used After Using the Heartstart OnsiteAfter Each USE Onsite Data StoragePhilips Medical Systems Reminders Routine MaintenanceMaintaining the Heartstart Onsite Periodic ChecksCleaning the Onsite Troubleshooting TipsDisposing of the Onsite REF 68-PCHAT Accessories for the Heartstart OnsitePhilips Medical Systems ECG Glossary of TermsAED CPRNSA Blinking green Ready light Periodic self-testsWaveform See Smart biphasic waveform See NSA pauseSCA Consciousness, absence of respiration, and lack of a pulseGlossary of SYMBOLS/CONTROLS Philips Medical Systems Symbol Philips Medical Systems Approved accessories are used Successful defibrillationOnSite on someone wearing an oxygen mask Precautions Environmental Heartstart Onsite Defibrillator SpecificationsTechnical Information PhysicalControls and Indicators Category SealingSee Electromagnetic Conformity tables Defibrillation Waveform DeliveredCurrent a Disarm AED mode Shock-to-shock cycle timeNewborn 14 J/kg ECG Analysis System ECG Analysis Performance Category Adult pads Infant/child pads Accessories SpecificationsBattery M5070A Category Battery type CapacityEnvironmental Considerations Appropriate recycling facilityRegulations Device Options ConfigurationPatient Treatment Protocol Options Pause, the OnSite returns to rhythm NSA pause type SettingsProtocol pause timer and CPR Coaching parameter settingsCPR4 Yes, No InstalledInfants and children when an infant Child pads cartridge is installedPhilips Medical Systems Recommended Action During AN Emergency Testing and TroubleshootingTesting TroubleshootingTroubleshooting While the Onsite is in USE Green Ready light is solid OnSite tells youTo insert a pads cartridge OnSite tells you To stop all motion Troubleshooting While the Onsite is not in USE Contact Philips for service if neededGreen Ready light is not on Behavior Cispr Electromagnetic ConformityElectromagnetic Emissions Emissions testESD Electromagnetic ImmunitySeparation distance according to frequency of transmitter m Important Warnings and Reminders Environmental ConsiderationsShock Cycle Timing Intentionally blank Intentionally blank Intentionally blank Latin America Philips Medical Systems United StatesCanada Europe, Middle East, and Africa
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M5066A specifications

The Philips M5066A is a state-of-the-art multi-parameter patient monitor designed to enhance healthcare delivery in various clinical settings. This versatile monitoring solution is widely utilized in hospitals, especially in critical care units and during transport, owing to its robust features and reliable performance.

One of the main features of the M5066A is its ability to monitor multiple vital signs simultaneously, including ECG, heart rate, invasive and non-invasive blood pressure, respiration rate, temperature, and saturation levels. This multi-parameter capability allows healthcare professionals to gain a comprehensive view of a patient’s health status, enabling timely interventions and improved patient outcomes.

The M5066A incorporates advanced technologies such as Philips’ proprietary IntelliVue technology, which enhances the accuracy and reliability of vital sign measurements. The monitor uses sophisticated algorithms to filter out noise and interferences, ensuring that the data presented to caregivers is both precise and actionable. The device also supports a range of connectivity options, allowing for seamless integration with hospital information systems and electronic medical records (EMRs). This connectivity facilitates the easy transfer and management of patient data, promoting better coordination of care.

Another significant characteristic of the M5066A is its user-friendly interface. The large, high-resolution display provides clear visuals of vital sign trends and parameters, enabling quick assessments by healthcare professionals. Customizable alarms and alerts can be programmed to suit specific patient needs, ensuring that caregivers are notified of critical changes in a timely manner.

The M5066A is also designed with patient comfort and safety in mind. The device's compact and lightweight design facilitates easy transport, while its durable construction ensures reliability in demanding environments. Furthermore, the monitor's battery backup allows for continuous monitoring even during power outages or when moving patients between departments.

In conclusion, the Philips M5066A multi-parameter patient monitor is a sophisticated tool that enhances patient monitoring by providing accurate, real-time data. Its advanced technologies, comprehensive monitoring capabilities, user-friendly interface, and focus on safety and comfort make it an invaluable asset in any clinical setting, helping healthcare providers deliver the highest standard of care.