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Summary of Contents for DHG Bure Rise & Go DB
- Page 1 Bure Rise & Go DB Instructions for use – English Max Patient Weight: 150 kg / 330 lbs IFU no: 936 rev. 1 2022-11-22...
- Page 2 Bure Rise & Go DB Instructions for use - English The Bure Rise & Go Double is an electrically operated Walker that is enhanced with a power rise function. The product consists of a Walker and its associated harness and straps. 1.
- Page 3 Warnings • The device may not be used by infants, children or adults who are 146 cm or shorter. • The caregiver must be able to read and understand the manual/Instructions for Use of the product. • Caregiver: Never use the device if you have not had a proper training on how to use the device including the accessories.
- Page 4 Before use: • Inspect the packaging for any damage. • Check for correct product being delivered. • Check to ensure that the device is free from damage. • Check if all the parts/components are included in the packaging. • Check if all approved accessories are included in the package. •...
- Page 5 3. Thread both attachment belts through the Walker’s frame and the green locking devices. Make sure the belts are threaded completely through the locking devices. NB: Check especially that the belts are undamaged. Check that belts are not worn or frayed and that the holder and straps are not bent or crooked.
- Page 6 Using Bure Walker with Gait training Kit 56-388 - KIT and Belt MULTI The walking training harness is an accessory used for increased safety when walking in the product Bure Rise & Go. The product’s both straps and fastening hooks minimize risks if patients suffer from dizziness or similar issues.
- Page 7 Raising/Lowering the Frame The desired height is adjusted with Arrow <UP> or Arrow <DOWN>. Adjust bottom frame using <WIDER> arrow or <NARROWER> arrow. Hand Control has charge indicator / battery (low, medium, high) and Service indicator. Service indicator – flashes red after 11 months’ operation. Constant light (red) after 12 months’...
- Page 8 Using the Parking Brakes on Castor Wheels: When parking the device, activate the parking brake on the lockable castor wheels. Lock the wheels by pressing the green pedal brake down with your foot. To release the brake, press the green protruding part with your foot. The caregiver should assist the patient in activating the parking brake in case the patient cannot activate them him or herself.
- Page 9 Battery Charging Battery charging must take place when the device is not in use. Charging starts automatically when power plug is connected to 230V wall socket. • LED lights YELLOW during charging (at the same time as the charging indi- cator on the hand control flashes yellow).
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Page 10: Maintenance
Repairs and maintenance may only be done by authorised personnel using original spare parts. • Power cord may only be replaced by DHG service personnel or technical personnel trained by DHG. • DHG can provide, upon request neccessary technical information in order to assist maintenace and repair of the device. - Page 11 1060 40°C Storage and transportation 5°C The walker should be transported and stored in 5°C to 50°C and in normal humidity, 20% to 80% non-condensing. The air pressure should be between 700 and 1060hPa. Leftmost symbol indicates storage and transportation. Let the walker reach room temperature before the batteries are charged or the walker is used.
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Page 12: Technical Specifications
5. Technical Specifications Linak, voltage 100V/240V, Max 1.5A, 50/60 Hz, IPX6, Class II (Double insulated) Control box Linak, 25,2V/2,1Ah, sealed,Li-Ion, 300mA IPX6, Cable length 200mm Batteries Linak, DC 24 V, 4,3A, IPX6. Duty cycle: Max 10% or 2 minutes continuous use Lifting Actuator followed by 18 minutes not in use, Push: 2000N. - Page 13 Accessories Part number Description 58-328-1 Heel strap Standing plate 56-336-4 Oxygen holder 56-338 Drip rod complete with attachment 56-337 Side support, adjustable 56-337-PU Side support, adjustable PU 56-352 Lower Leg Support 56-388 Gait training kit 56-388-KIT Gait training kit incl. brackets Multi Rise&Go 57-368-4 Guide handle 56-389...
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Page 14: Product Label
6. Product label UDI (Unique Device Identification) can be found within the barcode human readable text. It contains. (01) EAN code (11) Date of Manufacture. The date is in the format YYMMDD Y = Year, M = Month and D = Date. (21) Serial Number displayed as five digit code. - Page 15 7. Table of Symbols This product complies with the Visual Inspection requirements of the Medical Device Regulation 2017/745 Medical Device Read the manual Caution Product Code Legal manufacturer Batch Code Direct Healthcare Group Sverige AB Type BF applied parts, according to the The device is intended for indoor use degree of protection against electric shock WEEE Symbol...
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Page 16: Electromagnetic Compatibility (Emc)
Electromagnetic Compatibility (EMC) Electromagnetic emissions and test levels The product is intended to be used in the stated environments with electromagnetic levels as specified below. The caregiver and/or user of the product assure that the product is used in such an environment. Emission test Standards Compliance... - Page 17 Immunity test Basic EMC standard IEC 60601-1-2 Edition 4 Test levels and compliance or test method Professional healthcare facility Home healthcare environment environment Surge IEC 61000-4-5 ± 0.5 kV, ± 1 kV Voltage dips IEC 61000-4-11 0% U ; 0.5 cycle At 0°, 45°, 90°, 135°, 180°, 225°, 270°...
- Page 18 Radiated Radio – Frequency, Proximity fields from wireless communication equipment & compliance. (Dwell time: 3 sec.) Standard: IEC 61000-4-3 Test Frequency Band (MHz) Service Modulation I m m u n i t y (MHz) test levels (V/m) 380 to 390 TETRA 400 Pulse modulation 18 Hz...
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