1、07-10 11 73 00 - 1 SECTION 11 73 00 CEILING MOUNTED PATIENT LIFT SYSTEM SPEC WRITER NOTE: Delete between /-/ if not applicable to project. Also delete any other item or paragraph not applicable in the section and renumber the paragraphs. PART 1 - GENERAL 1.1 DESCRIPTION Ceiling Mounted Patient Lift
2、Systems for the transfer of physically challenged patients are specified in this section. 1.2 RELATED WORK A. Section 01 00 00, GENERAL REQUIREMENTS: Requirements for pre-test of equipment. B. Section 13 05 41, SEISMIC RESTRAINT REQUIREMENTS FOR NON-STRUCTURAL COMPONENTS: Seismic requirements for no
3、n-structural equipment. C. Section 26 05 11, REQUIREMENTS FOR ELECTRICAL INSTALLATIONS: General Electrical Requirements and items, which are common to sections of Division 26. 1.3 QUALITY ASSURANCE Certification for compliance is required for Ceiling Mounted Patient Lift Systems. Certifications shal
4、l be provided by an independent third party who will conduct testing to ensure that the ceiling lift and charging system are safe and in compliance with ISO 10535 & UL 60601-1 1.4 SUBMITTALS A. Submit in accordance with specification Section 01 33 23, SHOP DRAWINGS, PRODUCT DATA AND SAMPLES. B. Cert
5、ificates of Compliance C. Manufacturers Literature and Data: 1. Lifting Capacity 2. Lifting Speed 3. Horizontal Displacement Speeds 4. Horizontal Axis Motor 5. Vertical Axis Motor 6. Emergency Brake 7. Emergency Lowering Device 8. Emergency Stopping Device 9. Electronic Soft-Start and Soft-Stop Moto
6、r Control 10. Current Limiter for Circuit Protection 11. Low Battery Disconnect System 12. Strap Length Provided by IHSNot for ResaleNo reproduction or networking permitted without license from IHS-,-,-07-10 11 73 00 - 2 13. All equipment anchors and supports. Submittals shall include weights, dimen
7、sions, center of gravity, standard connections, manufacturers recommendations and behavior problems (e.g., vibration, thermal expansion,) associated with equipment or piping so that the proposed installation can be properly reviewed. D. Individual Room layouts showing location of lift system install
8、ation shall be approved before proceeding with installation of lifts. 1.5 APPLICABLE PUBLICATIONS A. The publications listed below form a part of this specification to the extent referenced. The publications are listed in the text by the basic designation only. B. International Organization for Stan
9、dardization (IOS): 10535-06 . Hoist for the Transfer of Disabled Persons-Requirements and Test Methods C. Underwriters Laboratories (UL): 60601-1 Medical Electrical Equipment: General Requirements for Safety 94-2006 UL Standards for Safety Test for Flammability of Plastic Materials for Parts in Devi
10、ces and Appliances-Fifth Edition D. International Electromagnetic Commission (IEC): 801-2(1991) Electromagnetic Compatibility for Industrial-Process Measurement and Control Equipment-Part 2: Electromagnetic Discharge Requirements PART 2 - PRODUCTS 2.1 CEILING TRACK SYSTEM The Ceiling Track shall be
11、made from high strength extruded aluminum T66081-T5 at a thickness of 3/16” (4.8mm). Provide anchor supports at a minimum 3 per linear foot at ceiling substrate. The ceiling track shall be finished with baked enamel paint. 2.2 LIFT UNIT A. The Lift Unit shall be constructed of a steel frame system (
12、2205lbs / 1000kg tested) driven by a gear reduced high torque motor B. The Lift system shall have the following features. 1. Lifting capacity: 440 lbs (200 kg) 2. Electronic soft-start and soft-stop motor control 3. Emergency lowering device 4. Emergency stopping device 5. Current limiter for circui
13、t protection in case of overload. Provided by IHSNot for ResaleNo reproduction or networking permitted without license from IHS-,-,-07-10 11 73 00 - 3 6. Safety device that stops the motor to lift when batteries are low. 7. Lifting speed: 2.3in/s (6 cm/s), 1.6in/s (3.5cm) in full capacity 8. Horizon
14、tal displacement speed: 5.9in/s (150mm/s) 9. Horizontal axis motor: 24VDC at 62 watts and vertical axis motor at 110 watts 10. Emergency brake (in case of mechanical failure) 11. Strap length up to 90in (2.3m) tested for 2998lbs (1360kg) 12. Cab: VO plasticfire retardant, UL 94 13. Wireless remote c
15、ontrol (optional) 2.3 MOTORS A. Vertical Movement-DC Motor 1. Type: Class A, fully enclosed, permanent magnet. 2. Rating: 24Vdc, 1.1A, 110W, 4000RPM, 0.3N-m. 3. Mounting: Secured to chassis. B. Horizontal Movement-DC Motor 1. Type: Fully enclosed, permanent magnet, integral reducer. 2. Rating: 24Vdc
16、, 1.8A, 62W, 260RPM, 1.0N-m. 3. Mounting: Secured to chassis. 2.4 BATTERIES A. The life cycle (number of charging cycles) for batteries shall be in compliance with IEC 801-2. B. Provide rechargeable batteries with up to 120 transfers with a load of 200lbs (74kg) and up to 70 transfers with its maxim
17、um load of 440lbs (200kg). 2.5 CHARGER A. Charger Input: 100-240 Vac, 50/60 Hz. B. Charger Output: 27 Vdc, 1 A max. C. Supplemental to the charger provide a clip on charging station with indicator lights. 2.6 STRAPS AND SLING A. The straps shall be made of threaded nylon. The straps shall ensure the
18、 patients safety by preventing the patient from falling out of the sling. B. The sling shall be made from a polyester/nylon net material that is pliable, breathable and easy to use. The sling shall cradle the body of the patient. Provided by IHSNot for ResaleNo reproduction or networking permitted w
19、ithout license from IHS-,-,-07-10 11 73 00 - 4 PART 3 - EXECUTION 3.1 INSTALLATION A. Install ceiling mounted patient lift system as per manufacturers instruction and under the supervision of manufacturers qualified representative and as shown on drawings. B. If the distance in between the suspended
20、 ceiling and anchors is more than 18” consult with manufacturer to determine if lateral braces will be required. 3.2 INSTRUCTION AND PERSONNEL TRAINING Training shall be provided for the required personnel to educate them on proper operation and maintenance for the lift system equipment. 3.3 TEST Co
21、nduct performance test, in the presence of the Resident Engineer and a manufacturers field representative, to show that the patient lift system equipment and control devices operate properly and in accordance with design and specification requirements. - - - E N D - - - Provided by IHSNot for ResaleNo reproduction or networking permitted without license from IHS-,-,-
