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SECTION 11730
PATIENT HANDLING EQUIPMENT


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Copyright 2017 - 2018 ARCAT, Inc. - All rights reserved

** NOTE TO SPECIFIER ** Hill-Rom Safe Patient Handling & Mobility Solutions; a divsion of Hill-Rom Architectural Products; operating room equipment and management systems, health care industry products and solutions.
This section is based on the products of Hill-Rom Architectural Products, which is located at:
1069 State Route 46 E.
Batesville, IN 47006
Toll Free Tel: 812-934-7777
Fax: 812-934-8189
Email: request info (hrc.likopm@hill-rom.com)
Web: https://construction.hill-rom.com





[ Click Here ] for additional information.

Hill-Rom is a leading worldwide manufacturer and provider of medical technologies and related services for the health care industry, including patient support systems, safe mobility and handling solutions, non-invasive therapeutic products for a variety of acute and chronic medical conditions, medical equipment rentals, surgical products and information technology solutions. Hill-Rom's comprehensive product and service offerings are used by health care providers across the health care continuum and around the world in hospitals, extended care facilities and home care settings to enhance the safety and quality of patient care.
Hill-Rom: Enhancing outcomes for patients and their caregivers.


  1. GENERAL

    1. SECTION INCLUDES

** NOTE TO SPECIFIER ** Delete items below not required for the project.

      1. Lift units.

      2. Overhead rail systems.

      3. Free standing rail systems.

      4. Mobile patient lifts.

      5. Accessories:

        1. Horizontal lifts.

        2. Slingbars.

        3. Slings and lift sheet.

    1. RELATED SECTIONS

      1. Section 10253 - Headwalls, Headboards and Bed Locators.

      2. Section 11721 - Medical Arms and Columns.

      3. Section 11722 - Patient Monitoring Equipment.

      4. Section 11731 - Hospital Beds and Stretchers.

      5. Section 11742 - Patient Examination Equipment.

      6. Section 11761 - Operating Room Equipment and Management Systems.

      7. Section 16725 - Health Care Communications and Monitoring Systems.

    2. REFERENCES

** NOTE TO SPECIFIER ** Delete references from the list below that are not actually required by the text of the edited section.

      1. American National Standards Institute (ANSI):

** NOTE TO SPECIFIER ** UL 60601-1 is the 2nd edition of the electrical safety standard; ANSI/AAMI ES60601-1 is the current 3rd edition

        1. ANSI/AAMI ES60601-1 - Medical Electrical Equipment - Part 1: General Requirements for Basic Safety and Essential Performance.

      1. American Society of Civil Engineers (ASCE):

        1. Standards for Seismic Forces as a suspended nonstructural system

      2. Association for the Advancement of Medical Instrumentation (AAMI).

      3. CSA Group (CSA):

        1. CAN/CSA C22.2 No.60601-1 - Medical Electrical Equipment - Part 1: General Requirements for Basic Safety and Essential Performance.

      4. European Standards (EN):

        1. EN 60601-1-2 - Medical electrical equipment - Part 1-2: General requirements for basic safety and essential performance - Collateral Standard: Electromagnetic disturbances - Requirements and tests.

      5. European Medical Devices Directive (MDD):

        1. MDD 93/42/EEC, for Class I products.

      6. International Building Code (IBC):

        1. Seismic Requirements.

      7. International Electrotechnical Commission (IEC):

        1. IEC 60601-1 - Medical Electrical Equipment - Part 1: General Requirements for Basic Safety and Essential Performance.

** NOTE TO SPECIFIER ** EN and IEC have the same content.

        1. IEC 60601-1-2 - Medical electrical equipment - Part 1-2: General requirements for basic safety and essential performance - Collateral Standard: Electromagnetic disturbances - Requirements and tests.

      1. International Organization for Standardization, (ISO):

        1. ISO 10535 - Hoists for the transfer of disabled persons - Requirements and test methods.

      2. National Fire Protection Association (NFPA):

        1. NFPA 70 - National Electrical Code.

      3. Underwriters Laboratories (UL):

        1. UL 60601-1 - Medical Electrical Equipment, Part 1: General Requirements for Safety.

    1. SUBMITTALS

      1. Submit under provisions of Section 01300.

      2. Product Data: Manufacturer's data sheets on each product to be used, including:

        1. Source quality certificates.

        2. Certificate of Compliance: ISO 10535.

        3. Pre-Installation Manual: Preparation instructions and recommendations.

        4. Installation Manual: Storage and handling requirements and recommendations.

        5. Installation Manual: Installation methods.

        6. Service Manual: Maintenance and operations data.

      3. Shop Drawings: Include system components, utility requirements and connections, relationship with adjacent construction. Include required clearances and access for servicing.

        1. Indicate general arrangement of lift equipment.

        2. Electrical requirements.

        3. Space requirements.

        4. Finishes of components.

        5. Provide installation template for work performed by others.

    2. QUALITY ASSURANCE

      1. Regulatory Requirements: Comply with requirements of authorities having jurisdiction and applicable codes at the location of the project.

      2. Manufacturer Qualifications: Minimum 5 years' experience manufacturing similar products.

      3. Installer Qualifications: Minimum 2 years' experience installing similar products, and certified by the equipment manufacturer.

    3. DELIVERY, STORAGE, AND HANDLING

      1. Deliver and store products in manufacturer's unopened packaging bearing the brand name and manufacturer's identification until ready for installation.

      2. Comply with manufacturer's recommendations for storage. Handle materials to avoid damage.

    4. PROJECT CONDITIONS

      1. Maintain environmental conditions (temperature, humidity, and ventilation) within limits recommended by manufacturer for optimum results. Do not store or install products under environmental conditions outside manufacturer's recommended limits.

    5. WARRANTY

      1. Provide manufacturer's standard limited warranty.

  1. PRODUCTS

    1. MANUFACTURERS

      1. Acceptable Manufacturer: Hill-Rom Safe Patient Handling & Mobility Solutions, a Division of Hill-Rom Architectural Products, which is located at: 1069 State Route 46 E.; Batesville, IN 47006; Toll Free Tel: 812-934-7777; Fax: 812-934-8189; Email: request info (hrc.likopm@hill-rom.com); Web: https://construction.hill-rom.com

** NOTE TO SPECIFIER ** Delete one of the following two paragraphs; coordinate with requirements of Division 1 section on product options and substitutions.

      1. Substitutions: Not permitted.

      2. Requests for substitutions will be considered in accordance with provisions of Section 01600.

** NOTE TO SPECIFIER ** Delete Article if not required. Delete features not required.

    1. PERFORMANCE REQUIREMENTS

      1. Must be designed for operation by only one caregiver.

      2. Must comply with all relevant areas of NFPA 70 - National Electric Code.

      3. Seismic Requirements: Comply with International Building Code, California Building Code (CBC), and American Society of Civil Engineers Standards for Seismic Forces as a suspended nonstructural system. Account for patient presence in system during earthquake event. Lift system, including rails, vertical support elements, bracing and substructure elements, must be capable of resisting imposed forces without failure or yielding of aluminum rail members.

        1. Patient Weight: Equal to maximum motor capacity as tabulated in Section 2.02, A1.1a and/or A2.1b.

        2. Lateral forces imposed by patient swing: Based on 15-degree offset, 30-degree arc, with patient suspended.

    2. LIFT UNITS

      1. Basis of Design: Likorall as manufactured by Liko, a Division of Hill-Rom Company, Inc.

** NOTE TO SPECIFIER ** Delete lift units not required.

        1. Likorall Lift Motor Model 200: 440lbs (200kg) lift capacity.

        2. Likorall Lift Motor Model 242: 440lbs (200kg) lift capacity.

        3. Likorall Lift Motor Model 243: 507lbs (230kg) lift capacity.

        4. Likorall Lift Motor Model 250: 550lbs (250kg) lift capacity.

        5. Standards Compliance:

          1. ANSI/AAMI ES60601-1.

          2. CAN/CSA C22.2 No. 606.1.

          3. CAN/CSA C22.2 No.60601-1.

          4. EN60601-1-2.

          5. IEC 60601-1-2.

          6. ISO 10535.

          7. UL60601-1.

        6. Lifting Speed: 2 in per sec (51 mm per sec).

        7. Lifting Interval: Minimum 70.9 to 82.7 in (180 to 2100 mm) height adjustable.

        8. Electric Motor: 24 V, 10 to 13 A, self-braking, motor driven worm gear.

          1. Sealed aluminum motor casing.

          2. Emergency Stop Button: On side of motor per ISO 4.3.12.

          3. Hydraulic Single Fault Safety Drum-(SFS): Automatically brakes free fall in case of motor axle malfunction.

          4. Safety Squeeze Protection (SSP): Directly beneath motor automatically stopping lifting operation once slingbar reaches maximum height.

          5. Built-In Self-Diagnostics: Includes overload and anti-twist strap protection.

          6. Motor Lift Strap: 2 in (51 mm) minimum width, with ten-fold safety load margin.

          7. Noise Level: Less than 52 dB per lift unit.

          8. Quick Release System: Q-Link option to connect the strap to the slingbar allowing different slingbar options.

        9. Emergency Lowering: Electrical or Mechanical as applicable to model.

          1. Electrical Emergency Raising and Lowering: Push buttons on side of lift motor casing.

          2. Electrical Emergency Stop and Lowering: Pull cord on side of the motor casing.

          3. Mechanical Emergency Lowering Device: Integrated with the lift strap. Must be in line with sling-bar with additional 48 in (1219 mm) of reel-mounted strap.

        10. Batteries: Two rechargeable 12V, 2.4 to 2.6 A, valve regulated, sealed, lead accumulator (gel-type batteries).

          1. Charge Level Indicators: Audible beep and lighted low battery indicator (ISO 4.3.14).

        11. Battery Charging:

** NOTE TO SPECIFIER ** Delete two of the three battery charging options below. In-Rail is only available for the Likorall Lift Motor Model 250.

          1. On-wall: Patient room wall mounted, 110 VAC, 40 to 60 Hz, max 0.6 A, splash-proof double insulated.

          2. Side-Rail (Multistation): 110 VAC, 40 to 60 Hz, max 0.6 A, splash-proof double insulated.

          3. In-Rail (Likorall Lift Motor Model 250 only): 100-240 VAC, 50 to 60 Hz, max 0.5 A, splash-proof double insulated.

        1. Hand Control:

          1. Connect on the side of motor via a round thread-locking DIN connector.

          2. Hand control with an LED light to indicate charging to a power source and/or an indication when batteries are charging or finished charging.

          3. Hand control with a back-side spring clamp to attach the hand control to the strap when the lift is not in use.

          4. Hand control with a back-side hook option to attach the hand control to the strap via a hang-up accessory when the lift is not in use.

      1. Basis of Design: LikoGuard as manufactured by Liko, a Division of Hill-Rom Company, Inc.

** NOTE TO SPECIFIER ** Delete Lift units not required.

        1. LikoGuard Lift Motor Model L: 600lbs (272kg) lift capacity.

        2. LikoGuard Lift Motor Model XL: 800lbs (363kg) lift capacity.

        3. Standards Compliance:

          1. ANSI/AAMI ES60601-1

          2. CAN/CSA C22.2 No. 606.1.

          3. CAN/CSA C22.2 No.60601-1

          4. EN60601-1-2.

          5. IEC 60601-1-2.

          6. ISO 10535.

          7. UL60601-1.

        4. Lifting Speed: 2 in per sec (51 mm per sec).

        5. Lifting Interval: Minimum 68 to 92 in (1727 to 2337 mm), depending on installation height 6-11/16 to 9-1/16 in (170 to 230 mm).

        6. Motor: 2 x 24 V, 2 x 10 A to 2 x 12.5 A self-braking, motor driven worm gear.

          1. Plastic motor casing.

          2. Protection Class: IPX4 (humidity resistance).

          3. Emergency Stop Button: On side of motor per ISO 4.3.12.

          4. Centrifugal Hook System: Automatically brakes free fall in case of motor/gearbox failure.

          5. Safety Squeeze Protection (SSP): Directly beneath motor automatically stopping lifting operation once slingbar reaches maximum height.

          6. Built-In Self-Diagnostics: Includes overload and anti-twist strap protection.

          7. Motor Lift Strap: 2 in (51 mm) minimum width, with a six-fold safety margin.

          8. Noise Level: Less than 70 dB per lift unit.

          9. Quick Release System: Q-Link option to connect the strap to the slingbar allowing different slingbar options.

          10. Emergency Stop Function: With strap connected to the bottom side of the motor casing, reachable from floor via Emergency strap.

        7. Emergency Lowering:

          1. Manual: Located on lift motor casing and reachable from floor via emergency strap.

          2. Electrical Emergency Raising and Lowering: Through push buttons located on the bottom of lift motor casing.

        8. Batteries: Rechargeable Lithium-Ion battery, 25.2 V at 4.2 A, with built in charger.

** NOTE TO SPECIFIER ** Delete charging option that is not required.

          1. Pendant Charging: Charger current 1.0 A.

          2. IRC Charging: 0.3 A.

          3. Charge Level Indicators: Audible beep and lighted low battery indicator (ISO 4.3.14).

        1. Battery Charging:

** NOTE TO SPECIFIER ** Delete one of the two battery charging options below.

          1. On-wall: Patient room wall mounted, 85 to 264 VAC, 47 to 63 Hz, max 0.9 A, splash-proof double insulated.

          2. In-Rail: 90 to 264 VAC, 47 to 63 Hz, max 1.2 A, splash-proof double insulated.

        1. Hand Control:

          1. Cable is adjustable in length up to 28 in (711 mm) and fixed to lift motor.

          2. LED light indication charging from a power source.

          3. LED light indication when batteries are charged.

** NOTE TO SPECIFIER ** Optional. Delete if not required.

          1. Back-side hook option to attach the hand control to the strap via a hang-up accessory when the lift is not in use.
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