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Tel: 86-22-60526161 

 
 

IMPORTANT INFORMATION REQUIRED BY THE FCC 

 
 
 
This device complies with Part 15 of the FCC Rules. Its operation is 
subject to the following two conditions: (1) This device may not cause 
harmful interference, and (2) this device must accept any interference 
received, including interference that may cause undesired operation. 
Changes or modifications not expressly approved by iHealth Labs Inc. 
would void the user’s authority to operate the product. 

NOTE: This product has been tested and found to comply with the limits 

for a Class B digital device, pursuant to Part 15 of the FCC Rules. 

These limits are designed to provide reasonable protection against 

harmful interference in a residential installation. This product 

generates, uses, and can radiate radio frequency energy and, if not 

installed and used in accordance with the instructions, may cause 

harmful interference to radio communications. However, there is no 

guarantee that interference will not occur in a particular installation. 

If this product does cause harmful interference to radio or television 

reception, which can be determined by turning the equipment off and 

on, the user is encouraged to try to correct the interference by one 

or more of the following measures: 

—Reorient or relocate the receiving antenna. 

—Increase the separation between the equipment and receiver. 

—Connect the equipment into an outlet on a circuit different from 

that to which the receiver is connected. 

—Consult the dealer or an experienced radio/TV technician for help. 

 

The SAR limit of USA (FCC) is 1.6 W/kg averaged over one gram of tissue. Device has also been tested 

against this SAR limit.

 

 

IC NOTICE 
 
The SAR limit of Canada (IC) is 1.6 W/kg averaged over one gram of tissue. Device has 
also been tested against this SAR limit. 
 

This Class B digital apparatus complies with Canadian ICES-003.   

Cet appareil numérique de la classe B est conforme à la norme NMB-003 du Canada. 

 

This product complies with Industry Canada. IC: RSS-247 
 
This device complies with Industry Canada licence-exempt RSS standard(s). Operation is 
subject to the following two conditions:   
(1)this device may not cause interference, and   
(2)this device must accept any interference, including interference  that may cause 

Summary of Contents for BPM1AE

Page 1: ...ealth App 3 Set Wi Fi 3 OPERATING PROCEDURES 4 Connecting The Cuff To The Monitor 4 Apply The Cuff 4 Body Posture 5 OPERATION INSTRUCTIONS 5 SPECIFICATIONS 6 GENERAL SAFETY AND PRECAUTIONS 7 BATTERY H...

Page 2: ...ent system It is designed to measure the systolic and diastolic blood pressures and pulse rate of an adult individual by using a technique in which an inflatable cuff is wrapped around the upper arm T...

Page 3: ...th App from the App Store iOS device or Google Play Android device Use keyword search terms iHealth BPM1AE or Blood Pressure Monitor Set Wi Fi Step 1 Press and hold the user2 key for 10s the monitor w...

Page 4: ...f tubing connector the monitor will turn on Apply The Cuff a Pull the cuff end through the metal loop positioning it outward away from your body b Place a bare arm through the cuff and position the cu...

Page 5: ...placed at the same level as your heart Note Blood pressure can be affected by the position of the cuff and your physiologic condition OPERATION INSTRUCTIONS a After applying the cuff and your body is...

Page 6: ...asurements SPECIFICATIONS 1 Product name Blood Pressure Monitor 2 Model BPM1AE 3 Classification Internally powered Type BF applied part IP20 No AP or APG Continuous operation 4 Machine size approx 4 7...

Page 7: ...ressure exceed 300 mmHg or maintained above15 mmHg for longer than 3 minutes of the bladder may cause ecchymoma of your arm 7 Consult your physician for any of the following situations a The applicati...

Page 8: ...ranges 15 Please do not share the cuff with any infectious person to avoid cross infection 16 This product should not be used as a USB device 17 If the determined blood pressure systolic or diastolic...

Page 9: ...charging If the cuff doesn t connect with the monitor press any key the door temperature outdoor tempetature if Wi Fi set done the battery valume and clock if Wi Fi set done will display on monitor If...

Page 10: ...ated range specified in part SPECIFICACIONS In this case you should consult a physician or check if your operation violated the instructions The technical alarm condition outside the rated range is pr...

Page 11: ...f supplication instructions and retest Body posture was not correct during testing Review body posture instructions and retest Speaking moving arm or body being angry excited or nervous during test Re...

Page 12: ...n the safety and performance characteristics for a minimum of 10 000 measurements or three years of usage and the cuff integrity is maintained after 1 000 open close cycles of the closure 10 The batte...

Page 13: ...cal authority or retailer for recycling advice Symbol for MANUFACTURER Symbol for COMPILES WITH MDD93 42 EEC REQUIREMENTS Symbol for DATE OF MANUFACTURE Symbol for SERIAL NUMBER Symbol for EUROPEAN RE...

Page 14: ...oduct does cause harmful interference to radio or television reception which can be determined by turning the equipment off and on the user is encouraged to try to correct the interference by one or m...

Page 15: ...r glementaires et certifications iHealth peuvent tre consult s via ce lien https www ihealthlabs eu support certifications OTHER STANDARDS AND COMPLIANCES The Blood Pressure Monitor corresponds to th...

Page 16: ...munity test levels Home Healthcare Environment Electrostatic Discharge IEC 61000 4 2 8 kV contact 2kV 4kV 8kV 15kV air Radiated RF EM field IEC 61000 4 3 10V m 80MHz 2 7GHz 80 AM at 1kHz Proximity fie...

Page 17: ...kV 100kHz repetition frequency Surges Line to line IEC 61000 4 5 0 5 kV 1 kV Surges Line to ground IEC 61000 4 5 0 5 kV 1 kV 2 kV Conducted disturbances induced by RF fields IEC 61000 4 6 3V 0 15MHz...

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