USER MANUAL Body Pro 2 WITHINGS
Thank you for using Withings Body Pro 2
This guide explains how to use your Withings Body Pro 2.
It applies to users in the United States of America
Federal law (USA) restricts this device to sale by or on the order of a licensed practitioner.
Important notice
Before using Withings Body Pro 2, review the information in this guide. You may also find this guide online at: https://www.withings.com/us/en/guides
Retain this documentation for future reference.
Installation instructions are available within the Onboarding Guide provided with this user guide.
Please contact Withings when in need of assistance, setting up, using or maintaining the device or to report unexpected operations or events.
Any serious incident related to the Withings Body Pro 2 should be reported to Withings and competent authorities in your country of residence.
Disclaimer
Information in this guide may change without notice.
WITHINGS,
Intended Use (United States Regions)
Withings Body Pro 2 is a connected smart scale providing the following wellness features:
- Measure weight
- Calculate Body Mass Index (BMI)
- Measure pulse rate
- Estimate vascular age
Additionally, Withings Body Pro 2 is intended:
- to measure body composition for weight management purposes, and to maintain healthy levels of muscle, bone and fat mass, and encourage healthy living.
- for the measurement of electrochemical skin conductance to aid in the assessment of sudomotor function.
The results are intended to be transmitted to the user via the companion app. The results are also transmitted to clinicians or researchers for remote review.
Withings Body Pro 2 is indicated for use in the general adult population.
Warnings & Safety notice
- The device is not intended to continuously monitor vital signs in critical conditions or where the nature of the variations is such that it could result in immediate danger to the user.
- The device does not provide alarms.
- Keep away from children and pets. Small parts may be inhaled or swallowed.
- Exposing the device to prolonged tint, dust or light (including sunlight) may reduce its life or damage it.
- Inspect electrodes for warping, surface damage or corrosion and check for any other form of damage.
- Do not use the device if it is damaged. Use of a damaged device could cause injury or equipment failure.
- Do not submerge the scale or any of the components in water.
- Do not try to repair or modify this equipment yourself. No service or repairs should be performed on the device other than the maintenance listed in this guide.
- Do not use accessories, detachable parts, or materials not described in the product guide.
- Avoid using the device on feet with poor skin integrity, such as cuts, wounds or damaged skin.
- No modification of this equipment is allowed.
- Use of accessories, transducers and cables other than those specified or provided by the manufacturer of this equipment could result in increased electromagnetic emissions or decreased electromagnetic immunity of this equipment and result in improper operation.
- Portable RF communications equipment (including peripherals such as antenna cables and external antennas) should be used no closer than 30~cm (12 inches) to any part of the device, including cables specified by the manufacturer. Otherwise, degradation of the performance of this equipment could result.
- Use of this equipment adjacent to or stacked with other equipment should be avoided because it could result in improper operation. If such use is necessary, this equipment and the other equipment should be observed to verify that they are operating normally.
- Do not interconnect this equipment with other equipment not described in the product guide.
- Follow operational and storage conditions as described in the technical specifications section of this guide. Otherwise, measurement results may be impacted.
Technical Specifications
Product Name: Withings Body Pro 2
Model: WBS14
Battery Life: 10 months typical use
Power Source: Four (4) alkaline cells - AAA
Heart Rate Measurement Range: 30 bpm to 230 bpm
Display: Color 2.8 inch LCD screen
Weight Withings Body Pro 2: 2.2kg
Operation time: 30 seconds
Parts in contact with the skin: Glass plate of the scale
Weight Units: Kilograms (kg), Pounds (lb), Stone (st lb)
Weight range: 5kg - 200kg | 11lb - 440lb | 1st - 31 st
Transport and storage conditions:
-10°C (14°F) - 50°C (122°F)
10% -90%
86kPa-106kPa
Max altitude: 2000 m
Operation conditions:
5^ (41°F) - 35°C (95°F)
20% - 80%
86kPa-106kPa
Max altitude: 2000 m
IP Protection level: IP22
Mode of operation: Continuous Operation
Minimum product life: 3 years
Please be aware that the stated 3-year product life of Withings scales represents a minimum lifespan under standard tested conditions. Withings products are designed to last: our scales are manufactured with care, and are provided with continual over-the-air firmware updates to avoid obsolescence. This is why with proper care and usage, our health products are likely to serve you reliably for much longer than the minimum product life. In fact, we're proud to share that 50% of our users are still actively using their Withings scales after 7 years.
Wireless Specifications
| Mode | Frequency Band (MHz) | Maximum Output Power (dBm) |
| BT LE | 2402-2480 | 5 dBm |
| WLAN | 2412-2462 | 16 dBm |
The wireless communication of the device is supported by BLE, WiFi and cellular communication. This communication is established between the device and the Withings application. The communication between the device and the Withings application is encrypted through an exchange of a paired key.
The communication latency between the device and the Withings application takes less than 10 seconds when the device and the smartphone are less than 16 feet (5 meters) apart.
The communication between the device and the Withings application is not modified with sources of interference located within 5 meters. Wireless coexistence has been tested in accordance with the following standards:
-ANSIC63.27:2017 and
- AAMI TIR69:2017/(R2020)
Electromagnetic disturbances have been tested in accordance with the standard ANSI AAMI IEC 60601-1-2:2014.
RF Statement
Medical electrical equipment needs special precautions regarding EMC and needs to be installed and put into service according to the EMC information provided in the accompanying documents.
Portable and mobile RF communications equipment can affect medical electrical equipment
Guidance and manufacturer's declaration-electromagnetic emissions
Withings Body Pro 2 is intended for use in the electromagnetic environment specified below. The customer or the user of the Withings Body Pro 2 should ensure that it is used in such an environment.
| Emissions Test | Compliance | Electromagnetic environment - guidance |
| CE emissions CISPR11 | Group 1 | The device uses RF energy only for its internal function. Therefore, its RF emissions are very low and are not likely to cause any interference in nearby electronic equipment. |
| RE emissions CISPR11 | Class B |
| Harmonic emissions IEC 61000-3-2 | N/A | The device is suitable for use in all establishments, including domestic establishments and those directly connected to the public low-voltage power supply network that supplies buildings used for domestic purpose. |
| Voltage fluctuations/Flicker emissions IEC 61000-3-3 | N/A |
Declaration: Electromagnetic emissions and immunity for equipment and systems that are not life-supporting and are specified for use only in a shielded location.
Declaration: Electromagnetic immunity
| The device is intended for use in the electromagnetic environment specified below. The customer or the user of the device should ensure that it is used in such an environment. |
| Immunity test | IEC 60601 Test Level | Compliance Level | Electromagnetic environment - guidance |
| Conducted RF | 3 Vrms | N/A | N/A |
| IEC 61000-4-6 | 150kHz to 80MHz | | |
| Radiated RF | 3 V/m | N/A | Portable and mobile RF communications equipment should be used no closer to any part of the equipment or system including cables than the recommended separation distance calculated from the equation applicable to the frequency of the transmitter. Interference may occur in the vicinity of equipment marked with the following symbol: # |
| IEC 61000-4-3 | 80 MHz to 2.5 GHz | | |
| Electrostatic discharge (ESD) | Contact: ±8 kV | Contact: ±8 kV | Floors should be wood, concrete, or ceramic tile. If floors are covered with synthetic material the relative humidity should be at least 30%. |
| IEC 61000-4-2 | Air: ±2 kV, ±4 kV, ±8 kV, ±15 kV | Air: ±2 kV, ±4 kV, ±8 kV, ±15 kV | |
| Electrical fast transient/burst | 2 kV for power supply lines | N/A | The main power quality should be of the kind used in a typical commercial or hospital environment |
| IEC 61000-4-8 | 1 kV for input/output lines | | |
| Surge IEC 61000-4-5 | 1 kV differential mode | line(s) to line(s): +/- 1kV | The main power quality should be of the kind used in a typical commercial or hospital environment |
| 2 kV common mode |
| Voltage dips, short interruptions and voltage variations on power supply | -5% UT (95% dip in UT) for 0.5 cycles, -40% UT (60% dip in UT) for 5 cycles, -70% UT (30% dip in UT) for 25 cycles, -5% UT (95% dip in UT) for 5 sec | N/A | The main power quality should be of the kind used in a typical commercial or hospital environment. If the user of the equipment or system requires continued operation during power main interruptions, it is recommended that the equipment or system be powered from an uninterruptible power supply or a battery. |
| input lines IEC 61000-4-11 |
| Power frequency (50/60Hz) | 30 A/m | 30 A/m | The power frequency magnetic field should be at levels characteristic of a typical location in a typical commercial or hospital environment. |
| magnetic field IEC 61000-4-8 | 50 Hz or 60 Hz | 50 Hz or 60 Hz | |
Federal Communication Commission Interference Statement
This device complies with part 15 of the FCC Rules. 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.
FCC Caution: Changes or modifications not expressly approved by the party responsible for compliance could void the user's authority to operate the equipment
This equipment 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 equipment 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 equipment 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.
IMPORTANT NOTE:
Radiation Exposure Statement: This equipment complies with FCC radiation exposure limits set forth for an uncontrolled environment.
This equipment should be installed and operated with a minimum distance of 20~cm between the radiator & your body.
This transmitter must not be co-located or operating in conjunction with any other antenna or transmitter.
Country Code selection feature to be disabled for products marketed to the US/CANADA.
Contains FCC ID: 2AAGMGM02SA
| MODE | FREQUENCY BAND (MHz) | MAXIMUM OUTPUT POWER (dBm) |
| LTE | 1710 - 1785 | 23 dBm |
| LTE | 880 - 915 | 23 dBm |
| LTE | 832 - 862 | 23 dBm |
| LTE | 703 - 748 | 23 dBm |
Disposal
Actuation of European directive 2012/19/EU, for reduction in use of dangerous substances in the electric and electronic device and for garbage disposal. The symbol applied on the device or its packaging means that at the end of its useful life, the product should not be disposed of with domestic waste. At the end of the device's useful life, the user must deliver it to a collection center for electric and electronic garbage, or return it to the retailer when purchasing a new device. Disposing of the product separately prevents possible negative environmental and health consequences deriving from inadequate disposal. It also allows the recovery of materials it is composed of to save energy and resources and avoid negative effects to the environment and health. In case of abusive disposal of devices by the user, will be applied administrative endorsements in compliance with current standards. The device and its parts must be disposed of as appropriate, in accordance with national or regional regulations.
? Need help?
withings.com/support
Security
Withings recommends that you add a passcode (personal identification number [PIN]), Face ID or Touch ID (fingerprint) to your phone to add a layer of security. It is important to secure your phone since you will be storing personal health information. Users will also receive additional update notifications on the device via the Withings application, and updates are delivered wirelessly, encouraging rapid adoption of the latest security fixes. Do not install the device on a smartphone that you do not own. Do not use a public Wi-Fi network you don't know. Use a trusted Wi-Fi network with your device. The Withings application is not intended to be used on a computer. No indication of anti-virus software is needed. Only use official app stores to download the Withings application. In case of doubt, use the link go.withings.com
Warranty
WithingsTM Two (2) Years Limited Warranty - Withings Body Pro 2 Withings, 2 rue Maurice Hartmann, 92130 Issy-les-Moulineaux, ("Withings") warrants the Withings-branded hardware product ("Withings Product") against defects in materials and workmanship when used normally in accordance with Withings' published guidelines for a period of TWO (2) YEARS from the date of original retail purchase by the end-user purchaser ("Warranty Period"). Withings' published guidelines include but are not limited to information contained in technical specifications, safety instructions or the quick start guide. Withings does not warrant that the operation of the Withings Product will be uninterrupted or error-free. Withings is not responsible for damage arising from failure to follow instructions relating to the Withings Product's use.
Withings is not responsible for damage arising from failure to follow instructions relating to the Withings Product's use.
Equipment Symbol Description
Do not dispose of this product as unsorted municipal waste, take it to electronic recycling.
Read the Instruction Manual before use
Direct Current
The CE labeling certifies that the product complies with the general safety and performance requirements of Regulation 2017/45
Medical device
Medical device manufacturer
Temperature range
Upper and lower limits of pressure
Upper and lower limits of relative humidity
Ingress of water or particulate matter
Type BF-Applied Part (glass plate)
Do not use if package is damaged and consult instructions for use
Caution
Regulatory Compliance Mark
Complies with FCC regulations
Unique device identifier
Serial number
The product is made with a mixture of materials from FSC-certified forests, recycled materials, and/or FSC-controlled wood.
Importer
Swiss Authorized Representative
Emergo Australia
Level 20, tower II, Darling Park, 201 Sussex Street, Sydney, NSW 2000, Australia
UK Responsible Person
Emergo Consulting (UK) Ltd c/o Cr360 - UL International
Compass House, Vision Park Histon
Cambridge CB24 9BZ - United Kingdom
GUIA DEL USUARIO
ES - REGIONES ESTADOS UNIDOS
Gracias por utilizes Withings Body Pro 2.
Technical Specifications
withings.com/support
Seguridad
CH REP Swiss Authorized Representative
Australian sponsor
Emergo Australia
Level 20, tower II, Darling Park, 201 Sussex Street, Sydney, NSW 2000, Australia
UK Responsible Person
Emergo Consulting (UK) Ltd c/o Cr360 - UL International
Compass House, Vision Park Histon
Cambridge CB24 9BZ - United Kingdom
USERGUIDE
ENGLISH - EUROPEAN REGIONS
Thank you for using Withings Body Pro 2
This guide explains how to use your Withings Body Pro 2.
It applies to users in the European Union, Switzerland and the United Kingdom.
Important notice
Before using Withings Body Pro 2, review the information in this guide. You may also find this guide online at: https:// www.withtings.com/us/en/guides
Retain this documentation for future reference.
Installation instructions are available within the Onboarding Guide provided with this user guide.
Please contact Withings when in need of assistance, setting up, using or maintaining the device or to report unexpected operations or events.
Any serious incident related to the Withings Body Pro 2 should be reported to Withings and competent authorities in your country of residence.
Disclaimer
Information in this guide may change without notice.
WITHHINGS,
Intended use (non United States regions)
Withings Body Pro 2 is a connected smart scale providing the following wellness features:
measure weight
calculate Body Mass Index (BMI)
measure body composition
- measure pulse rate
measure pulse wave velocity
- estimate vascular age
Additionally, Withings Body Pro 2 is intended to detect and follow-up peripheral autonomic neuropathies in an adult population by performing measurements on the feet, on intact skin or in the presence of damaged skin, such as, but not limited to, blisters, callosities or wounds.
CONTRAINDICATIONS:
Do not use the device if you have a cardiac pacemaker, an implantable cardioverter-defibrillator (ICD), or other implanted electronic devices.
- Self-diagnosis and self-treatment can be dangerous. Always consult your doctor in case of questions or doubts.
- If you are pregnant, accuracy may be impacted for body composition analysis, electrodermal activity score, vascular age. Consult your doctor during pregnancy.
- Misuse of the device can cause injury.
- Do not step on the scale with wet feet. Potential allergic reactions may occur due to contact with materials used in the device.
- The device is not intended to continuously monitor vital signs in critical conditions or where the nature of the variations is such that it could result in immediate danger to the user.
- The device does not provide alarms.
- Keep away from children and pets. Small parts may be inhaled or swallowed.
- Exposing the device to prolonged tint, dust or light (including sunlight) may reduce its life or damage it.
- Inspect electrodes for warping, surface damage or corrosion and check for any other form of damage.
- Do not use the device if it is damaged. Use of a damaged device could cause injury or equipment failure.
- Do not submerge the scale or any of the components in water.
- Do not try to repair or modify this equipment yourself. No service or repairs should be performed on the device other than the maintenance listed in this guide.
- Do not use accessories, detachable parts, or materials not described in the product guide.
- Use of accessories, transducers and cables other than those specified or provided by the manufacturer of this equipment could result in increased electromagnetic emissions or decreased electromagnetic immunity of this equipment and result in improper operation.
- Portable RF communications equipment (including peripherals such as antenna cables and external antennas) should be used no closer than 30~cm (12 inches) to any part of the device, including cables specified by the manufacturer. Otherwise, degradation of the performance of this equipment could result.
- Use of this equipment adjacent to or stacked with other equipment should be avoided because it could result in improper operation. If such use is necessary, this equipment and the other equipment should be observed to verify that they are operating normally.
- Do not interconnect this equipment with other equipment not described in the product guide.
- Follow operational and storage conditions as described in the technical specifications section of this guide. Otherwise, measurement results may be impacted.
- Avoid using the device on feet with poor skin integrity, such as cuts, wounds or damaged skin.
- No modification of this equipment is allowed.
- The use of medication with anticholinergic agents may impact Nerve Health Score results. Ask your doctor about the medications you take if you are not sure whether they have anticholinergic properties.
- Drinking alcohol 24 hours prior to taking a measurement may affect the results of the Nerve Health Score.
- Measurement results may be impacted in case of lower limb amputation.
- In case of severe lesions on the feet (such as ulcers), consult your doctor prior to use, as the performance of the measurement may be impacted.
Technical Specifications
Product Name: Withings Body Pro 2
Model: WBS14
Battery Life: 10 months typical use
Power Source: Four (4) alkaline cells - AAA
Heart Rate Measurement Range: 30 bpm to 230 bpm
Display: Color 2.8 inch LCD screen
Weight Withings Body Pro 2: 2.2kg
Operation time: 30 seconds
Parts in contact with the skin: Glass plate of the scale
Weight Units: Kilogramos (kg), Libras (lb), Stones (st lb)
Weight range: 5kg - 200kg | 11lb - 440lb | 1st - 31 st
Nerve Health Score measurement accuracy: <0.1%
Transport and storage conditions:
$$
\begin{array}{l} - 1 0 ^ {\circ} \mathrm {C} (1 4 ^ {\circ} \mathrm {F}) - 5 0 ^ {\circ} \mathrm {C} (1 2 2 ^ {\circ} \mathrm {F}) \ 10\% -90\% \ 8 6 k P a - 1 0 6 k P a \ \text {M a x i m u m} = 2 0 0 0 \mathrm {m} \ \end{array}
$$
Operation conditions:
$$
1 5 ^ {\circ} \mathrm {C} (4 1 ^ {\circ} \mathrm {F}) - 3 5 ^ {\circ} \mathrm {C} (9 5 ^ {\circ} \mathrm {F})
$$
$$
20 \% - 80 \%
$$
$$
8 6 k P a - 1 0 6 k P a
$$
$$
\text {M a x i m u m} = 2 0 0 0 \mathrm {m}
$$
IP Protection level: IP22
Mode of operation: Continuous Operation
Minimum product life: 3 years
Please be aware that the stated 3-year product life of Withings scales represents a minimum lifespan under standard tested conditions. Withings products are designed to last: our scales are manufactured with care, and are provided with continual over-the-air firmware updates to avoid obsolescence. This is why with proper care and usage, our health products are likely to serve you reliably for much longer than the minimum product life. In fact, we're proud to share that 50% of our users are still actively using their Withings scales after 7 years.
Wireless Specifications
Mode Frequency Band (MHz)
Maximum Output Conducted Power (dBm)
BT LE 2402-2480 5 dBm
WLAN 2412-2462 16 dBm
The wireless communication of the device is supported by BLE, WiFi and cellular communication. This communication is established between the device and the Withings application. The communication between the device and the Withings application is encrypted through an exchange of a paired key.
The communication latency between the device and the Withings application takes less than 10 seconds when the device and the smartphone are less than 16 feet (5 meters) apart.
The communication between the device and the Withings application is not modified with sources of interference located within 5 meters. Wireless coexistence has been tested in accordance with the following standards:
-ANSIC63.27:2017 and
Electromagnetic disturbances have been tested in accordance with the standard ANSI AAMI IEC 60601-1-2:2014.
e, 100
an 100
our 100
1282 ings.com/compliance
Withings Body Pro 2 contributes to an early detection of peripheral autonomic neuropathy. It facilitates patient screening and helps physicians treat the disease earlier and thus attenuate the impact of the disease on the population. It allows users to monitor disease advancement or regression. It also increases awareness of physiological conditions in the general user population.
Withings Body Pro 2 ability to accurately measure Electrochemical Skin Conductance (ESC), also known as Galvanic Skin Response (GSR), was validated in a clinical study by comparison with a reference device, the Sudoscan. The mean difference (resp. standard deviation of paired differences) was 1.6 (resp. 3.5).
RF Statement
Medical electrical equipment needs special precautions regarding EMC and needs to be installed and put into service according to the EMC information provided in the accompanying documents.
Portable and mobile RF communications equipment can affect medical electrical equipment.
Guidance and manufacturer's declaration-electromagnetic emissions
| Emissions Test | Compliance | Electromagnetic environment - guidance |
| CE emissions CISPR11 | Group 1 | The device uses RF energy only for its internal function. Therefore, its RF emissions are very low and are not likely to cause any interference in nearby electronic equipment. |
| RE emissions CISPR11 | Class B |
| Harmonic emissions IEC 61000-3-2 | N/A | The device is suitable for use in all establishments, including domestic establishments and those directly connected to the public low-voltage power supply network that supplies buildings used for domestic purpose. |
| Voltage fluctuations/Flicker emissions IEC 61000-3-3 | N/A |
Declaration: Electromagnetic emissions and immunity for equipment and systems that are not life-supporting and are specified for use only in a shielded location.
Declaration: Electromagnetic immunity
| The device is intended for use in the electromagnetic environment specified below. The customer or the user of the device should ensure that it is used in such an environment. |
| Immunity test | IEC 60601 Test Level | Compliance Level | Electromagnetic environment - guidance |
| Conducted RF | 3 Vrms | N/A | N/A |
| IEC 61000-4-6 | 150kHz to 80MHz | | |
| Radiated RF | 3 V/m | N/A | Portable and mobile RF communications equipment should be used no closer to any part of the equipment or system including cables than the recommended separation distance calculated from the equation applicable to the frequency of the transmitter. Interference may occur in the vicinity of equipment marked with the following symbol: #i |
| IEC 61000-4-3 | 80 MHz to 2.5 GHz | | |
| Electrostatic discharge (ESD) | Contact: ±8 kV | Contact: ±8 kV | Floors should be wood, concrete, or ceramic tile. If floors are covered with synthetic material the relative humidity should be at least 30%. |
| IEC 61000-4-2 | Air: ±2 kV, ±4 kV, ±8 kV, ±15 kV | Air: ±2 kV, ±4 kV, ±8 kV, ±15 kV | |
| Electrical fast transient/burst | 2 kV for power supply lines | N/A | The main power quality should be of the kind used in a typical commercial or hospital environment |
| IEC 61000-4-8 | 1 kV for input/output lines | | |
| Surge IEC 61000-4-5 | 1 kV differential mode | line(s) to line(s): +/- 1kV | The main power quality should be of the kind used in a typical commercial or hospital environment |
| 2 kV common mode | | |
| Voltage dips, short interruptions and voltage variations on power supply | -5% UT (95% dip in UT) for 0.5 cycles, -40% UT (60% dip in UT) for 5 cycles, -70% UT (30% dip in UT) for 25 cycles, -5% UT (95% dip in UT) for 5 sec | N/A | The main power quality should be of the kind used in a typical commercial or hospital environment. If the user of the equipment or system requires continued operation during power main interruptions, it is recommended that the equipment or system be powered from an uninterruptible power supply or a battery. |
| input lines IEC 61000-4-11 | | | |
| Power frequency (50/60Hz) | 30 A/m | 30 A/m | The power frequency magnetic field should be at levels characteristic of a typical location in a typical commercial or hospital environment. |
| magnetic field IEC 61000-4-8 | 50 Hz or 60 Hz | 50 Hz or 60 Hz | |
Disposal
Actuation of European directive 2012/19/EU, for reduction in use of dangerous substances in the electric and electronic device and for garbage disposal. The symbol applied on the device or its packaging means that at the end of its useful life, the product should not be disposed of with domestic waste. At the end of the device's useful life, the user must deliver it to a collection center for electric and electronic garbage, or return it to the retailer when purchasing a new device. Disposing of the product separately prevents possible negative environmental and health consequences deriving from inadequate disposal. It also allows the recovery of materials it is composed of to save energy and resources and avoid negative effects to the environment and health. In case of abusive disposal of devices by the user, will be applied administrative endorsements in compliance with current standards. The device and its parts must be disposed of as appropriate, in accordance with national or regional regulations.
Need help?
withings.com/support
Security
Withings recommends that you add a passcode (personal identification number [PIN]), Face ID or Touch ID (fingerprint) to your phone to add a layer of security. It is important to secure your phone since you will be storing personal health information. Users will also receive additional update notifications on the device via the Withings application, and updates are delivered wirelessly, encouraging rapid adoption of the latest security fixes. Do not install the device on a smartphone that you do not own. Do not use a public Wi-Fi network you don't know. Use a trusted Wi-Fi network with your device. The Withings application is not intended to be used on a computer. No indication of anti-virus software is needed. Only use official app stores to download the Withings application. In case of doubt, use the link go.withings.com
Warranty
WithingsTM Two (2) Years Limited Warranty - Withings Body Pro 2
Withings, 2 rue Maurice Hartmann, 92130 Issy-les-Moulineaux, ("Withings") warrants the Withings-branded hardware product («Withings Product») against defects in materials and workmanship when used normally in accordance with Withings' published guidelines for a period of TWO (2) YEARS from the date of original retail purchase by the end-user purchaser ("Warranty Period"). Withings' published guidelines include but are not limited to information contained in technical specifications, safety instructions or the quick start guide. Withings does not warrant that the operation of the Withings Product will be uninterrupted or error-free. Withings is not responsible for damage arising from failure to follow instructions relating to the Withings Product's use.
Equipement symbol description
Do not dispose of this product as unsorted municipal waste, take it to electronic recycling.
Read the Instruction Manual before use
Direct Current
The CE labeling certifies that the product complies with the general safety and performance requirements of Regulation 2017/45
Medical device
Medical device manufacturer
Temperature range
Upper and lower limits of pressure
Upper and lower limits of relative humidity
Ingress of water or particulate matter
Type BF-Applied Part (glass plate)
Do not use if package is damaged and consult instructions for use
Caution
Regulatory Compliance Mark
Complies with FCC regulations
Unique device identifier
Serial number
FSC
Importer
Swiss Authorized Representative
Australian sponsor
Emergo Australia
Level 20, tower II, Darling Park, 201 Sussex Street, Sydney, NSW 2000, Australia
UK Responsible Person
Emergo Consulting (UK) Ltd c/o Cr360 - UL International
Compass House, Vision Park Histon
Cambridge CB24 9BZ - United Kingdom
GUIDE UTILISATEUR
FRANÇAIS - RÉGIONS EUROPE
Specifications Techniques
Poids supportés : 5kg - 200kg I 11lb - 440lb I 1st - 31st
Wireless Specifications
Declaration: Electromagnetic immunity
withings.com/support
Securité
Level 20, tower II, Darling Park, 201 Sussex Street, Sydney, NSW 2000, Australia
UK Responsible Person
Emergo Consulting (UK) Ltd c/o Cr360 - UL International
Compass House, Vision Park Histon
Cambridge CB24 9BZ - United Kingdom
This guide can be found in the following languages here:
WITHINGS
Withings Body Pro 2 | Proactive Health Tracking © 2024 Withings. All rights reserved. Jan. 2024
support.withings.com - 2 rue Maurice Hartmann, 92130 Issy-les-Moulineaux, France
