RecoveryAir PRO Fully customizable pneumatic compression system. Your RecoveryAir PRO pneumatic compression system comes with a pump, a pair of compression boots, a blocker plug, a DC power adapter, and a carrying pouch for both the pump and boots. See Warnings on pg. 16 for important safety instructions.
Getting started 1. To turn on the RecoveryAir PRO pump, press and hold the power button. 2. To get started, put your boots on first before attaching them to the pump. This allows you to get into the most comfortable position and avoid any disruption in the air flow connection. 3. Next, plug in the connector from the boots into the pump. Make sure you hear a “click” so that you know the RecoveryAir PRO is fully connected, is plugged in, and there is a proper seal. 4.
Feature Callouts Buttons 3 Power Button Start/Pause/Stop Button 4-way Buttons Select Button
Settings (Adjustable Range) Indicators Pressure Setting Warning Indicator Adjustable Pressure Range (20-100 mmHg) in increments of 5 mmHg. Adjustable pressure changes in increments of 1 mmHg while in Gradient Setting. Indicator lights up solid ON or blinking when a device malfunction is detected Time Setting 10min-90min in steps of 5min or continuous.
RecoverAir PRO Programs About negative gradient for all programs: The RecoveryAir PRO’s unique true negative gradient of pressure sequentially travels up the limb from the foot toward the heart in four internal overlapping chambers. The spiraling overlap of chambers safely maximizes circulation. • • The pressure can be the same in two consecutive chambers, but the pump won’t allow a back chamber to have a higher pressure than a front chamber. The minimum pressure level of each chamber is 20 mmHg.
Chamber 4 Chamber 3 Chamber 2 Chamber 1 Figure 1 - Sequential Cycle Mode 6
RecoverAir PRO Programs Isolation preset program The Isolation program is recommended when needing to treat a specific, isolated area of your choosing. Isolation inflation cycle (ISO) The Isolation program provides targeted compression to a selected zone. • A directional massage is applied to a smaller, isolated area. • Inflation starts with the front chamber. • The next chamber starts to inflate after a few seconds.
Interval preset program The Interval program allows for a cycle to turn on and then off in a sequential selected amount of time. • A directional massage is applied with a sequential cycle, and alternates between intervals of being under treatment (Time On) and no treatment (Time Off). • Start by selecting the Time On (in minutes), the Time Off (in minutes), and the total Interval program time (in hours).
PRO Mode (Custom) The PRO Mode allows you to create a fully customized program that’s unique to you. • • You can use the Pretreatment program or you can choose from four inflation cycles: Sequential, Isolation, Wave, or Flow. During your treatment, you can change the treatment parameters, but you can’t change the selected inflation cycle and can’t turn the pre-selected program ON/OFF. Pretreatment (See Figure 3) • Pretreatment treats the proximal areas first.
Sequence 1 Sequence 2 Sequence 3 Figure 3 - Pretreatment Sequences Chamber 4 Chamber 3 Chamber 2 Chamber 1 Figure 4 - Wave Cycle Mode 10
PRO Mode (Custom) Flow inflation cycle • Four sequences exist within the Flow inflation cycle. Each sequence is determined by the last chamber inflated. • The Flow inflation cycle has an associated Frequency parameter, which determines the number of sequences within the cycle. • You can set the Frequency to be between 1 and 8. • The default Frequency setting is 2.
Superior, hygienic design The RecoveryAir PRO compression boots have non-porous medical grade material that helps prevent bacteria buildup and provides a resistant surface. Our internal overlapping chambers provide a smooth surface to clean, which means no wiping under chamber flaps where bacteria can build up. This also means no smells. How to Clean Here are simple steps to cleaning your RecoveryAir PRO compression boots: 1. 2. 3. 4. Unzip the boots completely and lay them on a flat surface.
Charging the RecoveryAir PRO 1. 2. 3. After turning off the pump, plug the power adapter into the charging port of the RecoveryAir PRO pump. You can continue to use the RecoveryAir PRO while charging. Charging is complete when all 3 LED lights of the LED battery indicator are lit. Traveling with your RecoveryAir PRO Compression System When traveling with your RecoveryAir PRO Compression System, we recommend: • Roll ● the hose tightly and slide it into the foot section of your garment.
Lock & unlock feature: 1. 2. To lock or unlock the pump, press and hold the select and up arrow at the same time. You will then see a padlock icon appear on the main screen. Factory reset You can perform a factory reset to change all customized programs back to the original default setting by following this easy step: 1. Press and hold the select and play/stop buttons.
Smart Features The RecoveryAir PRO also connects to the Therabody app via Bluetooth, giving you total control of your RecoveryAir PRO session from the convenience of your smartphone. Not only can you easily access options like individual chamber pressure, but you can create and share custom routines with your friends, clients, or patients directly from the app via text message or email. Scan the QR code to get started.
Important Safety Information Read all instructions before using the RecoveryAir PRO Compression System for the first time. Warning • • • • This system is intended for use by people in good health. This system is not recommended for people who have heart problems, or vascular problems, have a condition requiring the use of any medical device, or have any condition that may affect their normal well-being. If you are, or may be, pregnant, consult with your physician before use.
Caution • • • • • • • • • • • • • • • • • • • 17 Do not operate the RecoveryAir PRO Compression System while operating a vehicle. Do not store or transport the RecoveryAir PRO Compression System beyond the specified temperature, humidity, and atmospheric pressure range. Do not use the RecoveryAir PRO Compression System beyond the specified temperature range: 10 to 30°C (50 to 86°F). Do not use the RecoveryAir PRO Compression System beyond the specified humidity range: 30%rH–75%rH, non-condensing.
Labels The following labels and symbols appear on the pump, garments and/or packaging.
Label 19 Description Location Separate collection for waste electrical and electronic equipment Note: For more information about disposal of equipment, its parts and accessories, please contact your local distributor.
Indications for Use RecoveryAir is indicated for the temporary relief of minor muscle aches and pains, and for the temporary increase in circulation to the treated areas in people who are in good health. RecoveryAir simulates kneading and stroking of tissues by using an inflatable garment. Note • • • • The pump is “multi-voltage” and can be used for travel. An appropriate socket adapter must be used in countries with incompatible wall outlets. Use only RecoveryAir garments with the RecoveryAir pump.
Note Possible Cause Action One garment inflates but the second one does not. The second garment does not receive air. Examine its hoses for kinks, twists and folds. The pump stops working, the Status Indicator turns On in yellow. Hose is not connected properly to garment or pump, or prong plug is not inserted into unused air outlet. Examine and fasten all air connections. When treating only one limb, always plug the unused air outlet with the prong plug provided with the pump.
Bluetooth Wireless Technology Information Bluetooth Compliance Version 4.2 low energy Operating Frequency 2.402–2.480 GHz Output Power 0 dBm Operating Range 3-meter radius (line of sight) Network Topology Operation Antenna Type Modulation Type Data Rate Star - bus Slave Integrated chip type antenna Adaptive Frequency Hopping Over the air: 1 Mbit/second Application throughput: 0.
EMC Manufacturer Declarations Electromagnetic Compatibility (EMC) Statement for Home Healthcare Environment The RecoveryAir PRO system has been evaluated to international standard IEC 60601- 1-2 “General requirements for basic safety and essential performance - Collateral standard: Electromagnetic compatibility - Requirements and tests”.
Caution: Basic Safety and Essential Performance • • • • This system should not be used adjacent to or stacked with other equipment and that if adjacent or stacked use is necessary, this system should be observed to verify normal operation in the configuration in which it will be used.
Guidance and Manufacturer’s Declaration – Electromagnetic Immunity The RecoveryAir PRO device is intended for use in the electromagnetic environment specified below. The customer or the user of the device should assure that it is used in such an environment.
Guidance and Manufacturer’s Declaration – Electromagnetic Immunity The RecoveryAir PRO device is intended for use in the electromagnetic environment specified below. The customer or the user of the device should assure that it is used in such an environment. Immunity Test IEC 60601 Test Level Conducted 3 Vrms/m for Immunity 61000-4-6 0.15MHz to 80MHz Radiated Immunity 61000-4-3 Compliance Level Electromagnetic Environment - Guidance 3 Vrms/m for 0.
Recommended Separation Distances between Portable and Mobile RF Communication Equipment and the Device The RecoveryAir PRO device is intended for use in an electromagnetic environment in which radiated RF disturbances are controlled.
Reporting adverse events to FDA MedWatch is the Food and Drug Administration’s (FDA) program for reporting serious reactions, product quality problems, therapeutic inequivalence/failure, and product use errors with human medical products, including drugs, biologic products, medical devices, dietary supplements, infant formula, and cosmetics. If you think you or someone in your family has experienced a serious reaction to a medical product, you are encouraged to take the reporting form to your doctor.
FCC compliance 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. Changes or modifications not expressly approved by the party responsible for compliance could void the user’s authority to operate the equipment.
30
VJ Born in Los Angeles, CA. Designed for everybody.