SOURCES SOUGHT
65 -- SOURCES SOUGHT VANEC - BED BPA
- Notice Date
- 5/23/2019
- Notice Type
- Synopsis
- NAICS
- 339113
— Surgical Appliance and Supplies Manufacturing
- Contracting Office
- Department of Veterans Affairs;VISN 5 Contracting;849 International Drive;Linthicum MD 21090
- ZIP Code
- 21090
- Solicitation Number
- 36C24519Q0354
- Response Due
- 6/6/2019
- Archive Date
- 6/16/2019
- Point of Contact
- 410-691-7304
- Small Business Set-Aside
- N/A
- Description
- REQUIREMENT OVERVIEW The purpose of this Statement of Need is to outline the specifications and responsibilities in relation to the provision, integration, and implementation of hospital bed replacement at VA Medical Centers within Veterans Integrated Service Networks (VISNs) 1, 2, 4 and 5. The VA facilities shall require removal of the existing hospital beds (as needed) in the below locations, and installation and implementation of the new replacement beds and applicable equipment. The Vendor shall provide all necessary tools, equipment/hardware, installation, maintenance, warranty, and training in accordance with this SOW. The primary goals are to achieve enhancement of patient safety, standardization, safety protocols, reduction in labor, and overall improvement of patient care. In addition, these beds will expand the capacity and capability of current clinical workflow, improve patient safety and handling, increase patient satisfaction, and provide consistent and reliable end user experience at point of care. Critical Care DEFINITION: An powered adjustable hospital bed is a device intended for medical purposes that consists of a bed with a built-in electric motor and remote controls that can be operated to adjust the height and surface contour of the bed. The device includes movable and latchable side rails as well as surfaces (i.e., mattresses). Integratable with multiple bed accessories. Critical Care INTENDED USE: General-purpose powered adjustable hospital beds are used for an adult patient on an inpatient critical care unit for resting and sleeping, and also during recuperation and/or medical treatments (e.g., alternating pressure). Medical/Surgical DEFINITION: An powered adjustable hospital bed is a device intended for medical purposes that consists of a bed with a built-in electric motor and remote controls that can be operated to adjust the height and surface contour of the bed. The device includes movable and latchable side rails as well as surfaces (i.e., mattresses). Integratable with multiple bed accessories. Medical Surgical INTENDED USE: General-purpose powered adjustable hospital beds are used for an adult patient on an inpatient hospital and/or extended care unit for resting and sleeping, and also during recuperation and/or medical treatments (e.g., alternating pressure). Bariatric DEFINITION: A bariatric powered adjustable hospital bed is a device intended for medical purposes that consists of a bed with a built-in electric motor and remote controls that can be operated to adjust the height and surface contour of the bed. The device includes movable and latchable side rails as well as surfaces (i.e., mattresses). Integratable with multiple bed accessories. Bariatric INTENDED USE: General-purpose powered adjustable hospital beds are used for a bariatric adult patient on an inpatient unit for resting and sleeping, and also during recuperation and/or medical treatments (e.g., alternating pressure). Long-Term Care DEFINITION: A powered adjustable extended care bed is a device intended for care purposes that consists of a bed with a built-in electric motor and remote controls that can be operated to adjust the height and surface contour of the bed. The device includes removable and latch-able side rails as well as surfaces (i.e., mattresses). Integratable with multiple bed accessories. Long-Term Care INTENDED USE: General-purpose powered adjustable extended care beds are used for an adult patient on an extended care unit for resting and sleeping, and also during recuperation and/or medical treatments. All equipment shall be new, state of the art, and not recertified nor refurbished. VISN 1 Stations Maine VA Medical Center, 1 VA Center, Augusta, ME 04330 White River Junction VA Medical Center, 215 North Main Street, White River Junction, VT 05009 Edith Nourse Rogers Memorial Veterans Hospital, 200 Springs Road, Bedford, MA 01730 VA Boston Healthcare System - Brockton, 940 Belmont Street, Brockton, MA 02301 VA Boston Healthcare System - West Roxbury,1400 VFW Parkway, West Roxbury, MA 02132 VA Central Western Massachusetts Healthcare System, 421 North Main Street, Leeds, MA 01053 VA Connecticut Healthcare System - West Haven, 950 Campbell Avenue, West Haven, CT 06516 VISN 2 Stations New York/New Jersey VA Health Care Network, 130 W. Kingsbridge Road, Building 16, Bronx, NY 10468 VA Western New York Healthcare System Buffalo, 3495 Bailey Avenue, Buffalo, NY 14215 Batavia VA Medical Center, 222 Richmond Avenue, Batavia, NY 14020-1227 Canandaigua VA Medical Center, 400 Fort Hill Avenue, Canandaigua, NY 14424 Bath VA Medical Center, 76 Veterans Avenue, Bath, NY 14810 Syracuse VA Medical Center, 800 Irving Avenue, Syracuse, NY 13210 Albany Stratton VA Medical Center, 113 Holland Avenue, Albany, NY 12208 VA New Jersey Healthcare System - East Orange385 Tremont Avenue, East Orange, NJ 07018 VA Hudson Valley Healthcare System - Castle Point 41 Castle Point Rd, Wappingers Falls, NY 12590 VA Hudson Valley Healthcare System - Montrose2094 Albany Post Road, Montrose, NY 10548 VA NY Harbor Healthcare System - Brooklyn800 Poly Place, Brooklyn, NY 11209 Northport VA Medical Center, 79 Middleville Road,Northport, NY 11768 VISN 4 Stations Altoona VA Medical Center, 2907 Pleasant Valley Blvd, Altoona, PA 16602 Butler VA Health Care System, 353 North Duffy Road, Butler, PA 16001 Coatesville Veterans Affairs Medical Center, 1400 Blackhorse Hill Road, Coatesville, PA 19320 Erie VA Medical Center, 135 East 38th Street Boulevard, Erie, PA 16504 Lebanon VA Medical Center, 1700 South Lincoln Avenue, Lebanon, PA 17042 Corporal Michael J. Crescenz VA Medical Center, 3900 Woodland Avenue, Philadelphia, PA 19104 VA Pittsburgh Healthcare System - University Drive, University Drive, Pittsburgh, PA 15240 VA Pittsburgh Healthcare System - H.J. Heinz, 1010 Delafield Road, Pittsburgh, PA 15215 Wilkes-Barre VA Medical Center, 1111 East End Blvd., Wilkes-Barre, PA 18711 VISN 5 Stations VA Maryland Healthcare System, 10 N Greene St, Baltimore, MD 21201 Perry Point VA Medical Center, 515 Broad Street, Perry Point, MD 21902-9998 Loch Raven VA Medical Center, 3901 The Alameda, Baltimore, MD 21218-2100 Beckley VA Medical Center, 200 Veterans Ave, Beckley WV 25801-6444 Louis A. Johnson VA Medical Center, 1 Medical Center Drive, Clarksburg WV 26301 Hershel "Woody" Williams VA Medical Center, 1540 Spring Valley Drive, Huntington WV 25704 Martinsburg VA Medical Center, 510 Butler Avenue, Martinsburg WV 25405 Washington DC VA Medical Center, 50 Irving Street, NW, Washington DC 20422 BED REQUIREMENTS Bed frame general requirements Bed shall accept a variety of surfaces (i.e., mattresses) that reduce pressure, shear, friction and moisture. The bed will be manufactured to avoid injuries (i.e., pinch points, skin tears). A list of all compatible surfaces (i.e., mattresses) shall be provided that includes: manufacturer, model, mattress type, dimensions (i.e., length, width, and height), and patient weight capacity. Bed frame with a compatible surface (i.e., mattress) shall meet U.S. Food and Drug Administration s (FDA s) Guidance for Industry and FDA Staff: Hospital Bed System Dimensional and Assessment Guidance to Reduce Entrapment, issued on March 10, 2006, which includes the following dimensional limits: Zone 1 (within the rail) less than 120mm; Zone 2 (under the rail, between rail supports or next to a single rail support) less than 120mm; Zone 3 (between rail and mattress) less than 120mm; Zone 4 (under the rail at the ends of the rail) less than 60mm AND greater than 60 ° angle. Open architectural frame that will accept any emergency evacuation device. Bed frame with a compatible surface (i.e., mattress) shall meet the IEC/EN 60601-2-52 bed standard, which includes the following additional dimensional limits: Zone 5 (between split bed rails) less than 120 mm or greater than 318 mm; Zone 6 (between the end of the rail and the side edge of the head or foot board) less than 120 mm; Zone 7 (between the head or foot board and the mattress end) less than 120 mm. Bed deck shall not contain springs. Mattress air pump shall be integrated into bed frame. All bed casters should be steerable and dual-locking. Bed casters should be at least 5 inches in diameter. Bed floor-to-frame clearance should be no less than 4.5 inches before any options are installed. Bed should be compatible with 120V AC power, be supplied with a hospital-grade NEMA 5-15P style power plug, and have a straight, uncoiled cord. Bed should be equipped with all cabling required to integrate with headwall. Critical Care beds should have bumpers at all four (4) corners to prevent impact damage. Bed frame dimension requirements Bed length shall be no less than 80 inches and no more than 95 inches Bed length shall be electronically adjustable to an additional 12 inches ( ± 2 inches) without use of tools or additional parts. Bed should be width adjustable such that the maximum width of the bed is between 40 inches and 53 inches wide. Bed shall have a fully motorized general-purpose electric bed frame capable of adjusting bed height and surface position. Bed deck shall descend to a minimum height of 16 inches and rise to a height of 30 inches. Weight Requirements Critical Care, Medical/Surgical and Long-term care beds shall support a patient weight of 500 pounds. Bariatric beds shall support a patient weight of 1000 pounds. Bed shall be prominently labeled to identify maximum patient weight capacity. Rail Requirements End rails (i.e., headboard and footboard) shall be removable without the use of tools. Side rails shall be attached to the bed frame Side rails shall be single hand release and able to be manually raised and lowered, and may be full length, half-length or quarter length. Rails shall not impede patient positioning, mobility, and comfort. Operation or removal of bed rails shall not create pinch points or sharp edges. Rails should be rated to the max capacity of the bed Control Requirements Bed shall have separate controls for the patient and the hospital staff (e.g., nurse or caregiver). Bed controls shall be integrated into the side rail(s) or contained within a separate hand pendant and are identified with words or symbols. Bed controls shall be sealed against fluid penetration. Bed controls shall be of the momentary-contact type. Bed controls shall NOT be of the walk-away type. Bed remote control should be physically attached to the frame. Bed controls shall include controls for patient lockout and special bed positions (e.g. Trendelenburg, Reverse Trendelenburg, Chair). Caregiver bed controls shall have lockout switches that are inaccessible to the patient and disable the patient bed controls. Bed controls shall be illuminated and identified with clearly visible symbols that allows for ease of use. Feature Requirements Bed shall have a cardiopulmonary resuscitation (CPR) control function that within 10 seconds (i.e., a period of time of no more than 10 seconds) adjusts the bed to a flat and stable position for the administration of CPR in the event of an emergency. CPR function/quick release is clearly marked, at the head of the bed, on the right and left sides and is not power dependent. CPR function shall be accessible without moving the patient, side or end rails, or any other accessory or component attached to the bed frame. CPR function shall be easily engaged using only one hand in a single motion. Bed shall have an exit-alarm feature. Bed Exit Alarms shall only be able to be engaged and disengaged by staff; patient shall not have accessibility. Bed Exit Alarms shall have an audible alarm and can be integrated into a hospital communication/call system (Reference Nurse Call Table under letter J) in which the alarm will sound via the call system at a central station and a call light will illuminate over the patient room door. Nurse Call feature shall be clearly visible with symbols and/or text, and easily accessible to the patient. Nurse Call feature may be integrated into the side rails and/or contained in a separate hand held pendant. Bed integrated patient scale shall measure to weight capacity of bed. Bed should be optioned with an integrated scale that measures in both pounds and kilograms. Integrated scale should measure patient weight in any position and have an accuracy within 5% of the patient's actual body weight. Further, repeatability of weight measurements should be within 5% of the previously recorded weight measurement. Bed shall have an automatic contour feature (also referred to as auto-contour and automatic knee break) that simultaneously bends the knee section of the bed when the head section is raised. Bed shall self-adjust to prevent patient migration with head elevation. Bed shall be retractable such that the foot end moves toward the head of the bed when the head section is raised. Critical Care, Medical/Surgical and Bariatric beds shall have integrated power assist drive. Bed should have built in 120 V power outlet. Bed shall have a battery memory/volume that would hold during transport and that would accommodate of other powered equipment during transport and at end location. Bed shall have a feature (e.g. neutral) for ease in transporting and is not dependent on power. Bed shall allow for transportation in an elevated position. Bed shall have a central brake system that is engaged and disengaged by foot control. Bed shall have safety locking mechanism/alert for brakes. Bed shall be capable of special bed positions, such as the chair /cardiac chair position or Trendelenburg/Reverse Trendelenburg. Bed should have chair and side egress for increased mobility. Changes in bed positions shall be conducted using electrical controls (i.e., head of bed and foot of bed are raised or lowered via use of bed controls). Bed should allow lifts and other equipment beneath the bed deck in multiple positions. Bed should have at least two (2) IV Pole Holders. Bed shall have separate anchors clearly marked and designed for restraints. All accessory attachment points must be clearly marked and dedicated for intended use. Bed should have a nightlight which enables interaction with bed controls without need for external lighting. Critical Care beds should have a removable pendant with caregiver controls for use by the caregiver to adjust bed settings. Critical Care, Medical/Surgical and Bariatric beds should have foot of bed controls with a patient lockout feature. Position Requirements Powered low chair positioning/Chair Setting Bed should electrically retract & extend Bed should be adjustable such that Trendelenburg and reverse-Trendelenburg elevations are at least +/- 10 degrees from parallel. Cleaning Requirements Bed shall be able to be cleaned using the Centers for Disease Control and Prevention (CDC) recommended 10% bleach cleaning solution for disinfection. Bed frame shall withstand heat of 160 ° for up to 4 hours Standard Regulation Requirements Bed shall meet ANSI/AAMI/IEC 60601-2:2007/(R) 2012, or equivalent electrical safety standard, that applies to the basic safety and essential performance of medical electrical equipment and medical electrical systems. Medical device manufacturer shall be a registered establishment with the U.S. Food and Drug Administration (FDA) in accordance with 21 CFR Part 807. Medical device shall be listed with U.S. Food and Drug Administration (FDA) in accordance with 21 CFR Part 807. Medical device shall be classified by U.S. Food and Drug Administration (FDA) under AC-powered Adjustable Hospital Bed in accordance with 21 CFR § 880.5100 MATTRESS REQUIREMENTS Low-Air-Loss, Alternating Pressure, Powered Adjustable Mattress General Requirements Mattress shall provide pressure redistribution via cyclic changes in loading and unloading as characterized by frequency, duration, amplitude and rate of change parameters. Surface/Mattress should provide a flow of air to assist in managing heat and micro climate of skin. Mattress shall consist of multiple air cells that can be filled and emptied in an alternating pattern by an associated control unit to provide regular, frequent, and automatic changes in the distribution of body pressure. Mattress shall have powered pressure redistribution and the functionally equivalent effect of supporting a patient and avoiding excess pressure on local body areas. Surface shall reduce friction and shear. A list of all compatible bed frames shall be provided that includes: manufacturer, model, mattress type, dimensions (i.e., length, width, and height), and patient weight capacity. Surface (i.e., mattress) with a compatible bedframe shall meet U.S. Food and Drug Administration s (FDA s) Guidance for Industry and FDA Staff: Hospital Bed System Dimensional and Assessment Guidance to Reduce Entrapment, issued on March 10, 2006, which includes the following dimensional limits: Zone 1 (within the rail) less than 120mm; Zone 2 (under the rail, between rail supports or next to a single rail support) less than 120mm; Zone 3 (between rail and mattress) less than 120mm; Zone 4 (under the rail at the ends of the rail) less than 60mm AND greater than 60 ° angle. Surface (i.e., mattress) with a compatible bedframe shall meet the IEC/EN 60601-2-52 bed standard, which includes the following additional dimensional limits: Zone 5 (between split bed rails) less than 120 mm or greater than 318 mm; Zone 6 (between the end of the rail and the side edge of the head or foot board) less than 120 mm; Zone 7 (between the head or foot board and the mattress end) less than 120 mm. Non-Powered Pressure Redistribution Mattress General Requirements Mattress shall have non-powered pressure redistribution and the functionally equivalent effect of supporting a patient and avoiding excess pressure on local body areas. Surface shall reduce friction and shear. A list of all compatible bed frames shall be provided that includes: manufacturer, model, mattress type, dimensions (i.e., length, width, and height), and patient weight capacity. Surface (i.e., mattress) with a compatible bedframe shall meet U.S. Food and Drug Administration s (FDA s) Guidance for Industry and FDA Staff: Hospital Bed System Dimensional and Assessment Guidance to Reduce Entrapment, issued on March 10, 2006, which includes the following dimensional limits: Zone 1 (within the rail) less than 120mm; Zone 2 (under the rail, between rail supports or next to a single rail support) less than 120mm; Zone 3 (between rail and mattress) less than 120mm; Zone 4 (under the rail at the ends of the rail) less than 60mm AND greater than 60 ° angle. Surface (i.e., mattress) with a compatible bedframe shall meet the IEC/EN 60601-2-52 bed standard, which includes the following additional dimensional limits: Zone 5 (between split bed rails) less than 120 mm or greater than 318 mm; Zone 6 (between the end of the rail and the side edge of the head or foot board) less than 120 mm; Zone 7 (between the head or foot board and the mattress end) less than 120 mm. ALL Mattress Dimension Requirements Mattress length shall be no less than 80 inches. Mattress width shall be no less than 36 inches. Mattress height when fully inflated shall be no less than 5 inches. Mattress height when fully inflated shall not exceed 10 inches and not raise equal to or exceed the height of the side rails. ALL Mattress Weight Requirements Critical Care, Medical/Surgical and Long-term Mattress shall support a patient weight of 500 pounds. Bariatric Mattress shall support a patient weight of 1000 pounds. Mattress shall be prominently labeled to identify maximum patient weight capacity. ALL Mattress Cover Requirements Surface cover shall be bacteria resistant, flame retardant, fluid impenetrable, anti-fungal, anti-static, non-allergenic and non-shearing. Surface cover shall be wipe-able without requiring laundering. Low-Air-Loss, Alternating Pressure, Powered Adjustable Mattress Control Requirements Mattress controls shall regulate the temperature of the blown air if applicable. Mattress controls shall be easily accessible by patient care provider. Mattress control settings shall be adjustable. Mattress controls shall have lockout switches that are inaccessible to the patient. Mattress controls shall be illuminated and clearly visible. Low-Air-Loss, Alternating Pressure, Powered Adjustable Mattress Feature Requirements Mattress shall have a cardiopulmonary resuscitation (CPR) control function that quickly (i.e., a period of time of no more than 10 seconds) adjusts the bed to a flat and hard/stable position for the administration of CPR in the event of an emergency. CPR function/quick release is clearly marked and is not power dependent. CPR function shall be accessible without moving the patient, side or end rails, or any other accessory or component attached to the surface. CPR function shall be easily engaged using only one hand in a single motion. Surface and mattress interior and exterior shall be free of latex and toxins, including but not limited to: cadmium, mercury, asbestos, PVC/DEHP, PCB, and CFC. Mattress shall not inhibit or restrict the ability to raise and lower the side rails of the bed frame. Mattress temperature of the blown air shall not exceed 105 °F. Mattress shall have an input air filter. Mattress should be max inflated in thirty (30) seconds or less. Mattress shall utilize 100-150 liters of air per minute to maintain normal skin temperature and moisture levels. Mattress shall redistribute weight uniformly, reduce pressure to that of below capillary closure, and circulate air across the skin to reduce moisture. Mattress should have powered turn assist capability. Mattress shall contain foam, or another equivalent pressure reducing product, at the base (beneath the cells) that allows some continuation of pressure reduction in the event of an extended mechanical or electrical failure. Mattress operational noise levels shall not exceed 35dB. Mattress, when bed is placed in Fowlers/Sitting position, cells shall not loose functionality and integrity. Mattress, when inflated, shall prevent 'bottoming out'. Mattress shall have 'bolsters' to assist with transfers/getting out of bed, but also to prevent patient from 'rolling out' due to softness. Mattress pressure at heel area should be less than head area. Mattress should remain inflated for 12 hours without power. Mattress shall alert hospital staff when the system is not functioning within the manufactures' published specifications (e.g., power loss, air temperature too high, pressure level too low, etc.). Mattress shall have battery backup (or some other feature) to allow for continuous functioning of the mattress during transport and power outages. Non-Powered Pressure Redistribution Mattress Feature Requirements Surface and mattress interior and exterior shall be free of latex and toxins, including but not limited to: cadmium, mercury, asbestos, PVC/DEHP, PCB, and CFC. Mattress may be multi-zoned (i.e., a mattress that has different segments that have different pressure distribution characteristics to help reduce the development of bed sores in areas where they are most likely to develop, such as the head, body and foot) to match the body s proportional differences maximizing pressure redistribution to the head, body and foot. Mattress and/or surface shall not inhibit or restrict the ability to raise and lower the side rails of the bed frame. Mattress shall be compatible with bed exit alarms so as not to compromise alarm function. Mattress should contain non-powered air support chambers or cylinders, which can be manually adjusted via use of a pump, but are not dependent upon power to maintain pressure reduction. Mattress shall not slip, slide or migrate when bed is placed in fowlers or Trendelenburg positions. All Mattress Cleaning Requirements Surface must be cleanable and disinfectable by EPA approved cleaning and disinfection products. Surface shall be able to be cleaned using the Centers for Disease Control and Prevention (CDC) recommended 10% bleach cleaning solution for disinfection. Mattress surface shall withstand heat of 160 ° for up to 4 hours. Mattress controls shall be illuminated and clearly visible. All Mattress Standard Regulation Requirements Surface shall meet all State and Federal safety standards which includes fire regulations. Surface shall meet the standards for the flammability of mattress sets (i.e., 16 CFR Part 1633, 16 CFR Part 1632). Surface shall be labeled in accordance with U.S. Food and Drug Administration s (FDA s) guidance for Recommendations for Labeling Medical Products to Inform Users that the Product or Product Container is not Made with Natural Rubber Latex issued on December 2, 2014. Medical device manufacturer shall be a registered establishment with the U.S. Food and Drug Administration (FDA) in accordance with 21 CFR Part 807. Medical device shall be listed with U.S. Food and Drug Administration (FDA) in accordance with 21 CFR Part 807. Medical device shall be classified by U.S. Food and Drug Administration (FDA) under non-powered flotation therapy mattress in accordance with 21 CFR § 880.5150. BED ACCESSORIES Please provide a list of all hospital bed accessories available including but not limited to (each accessory should not require specific tools for assembly or attachment): Oxygen tank holder designed for bed with flexibility (i.e. swinging capability) IV poles and securing brackets Foley bag, chest tube, fecal management collector, etc. hooks Over bed tables that are compatible in all positions Removable headboard designed for CPR use if available Overhead patient assistance device (i.e. trapeze) shall be adjustable, secure and able to be disinfected. When designed for bariatric use, Max load to be defined. Additional surface cover Patient comfort items: USP Port, AUX Port, Any options available Beds shall interface with TV s with side rail controls/remote that can be stored within the bed rails. Option of CIS/ARK Integration Transport table Diagnostic tools and equipment necessary to provide service and maintenance Retractable power cord TRAINING REQUIREMENTS Clinical training: The Vendor shall provide on-site clinical applications training during initial setup as well as follow up training. Technical training: The Vendor shall provide technical training during initial setup and operations of the equipment, as well as follow-up training during everyday operation. Additionally, the Vendor will provide two tuition-free OEM technical training courses to be completed at manufacturer training facility. WARRANTY AND SERVICE REQUIREMENTS Service and Operator Manuals The vendor shall provide the following documentation for the proposed systems: Two (2) copies (one (1) electronic and one (1) physical copy), per medical facility, of operator's instruction manuals per model purchased Two (2) copies (one (1) electronic and one (1) physical copy), per medical facility, of complete technical service manuals including detailed troubleshooting guides, necessary diagnostic software, service keys, schematic diagrams, and parts lists. Minimum Warranty The system and accessories shall be covered under the manufacturer s warranty and shall include all parts and labor for a minimum of two years following acceptance by the VA Medical Center (VAMC). The manufacturer s factory-trained field service personnel shall perform installation and maintenance during the warranty period. The warranty period shall not begin until after VAMC authorized personnel have accepted the products delivery, installation, and functionality. Vendors are encouraged to include any offerings for service, warranty, and training that may exceed the requirements with their proposals. Vendors who do not include any added value offerings for service, warranty, and training will not be docked or excluded from consideration. However, any such offerings will be evaluated based on added value. SUPPORT / MAINTENANCE Vendor shall provide service/maintenance agreement for 8am-6pm EST coverage and provide 24/7 technical and clinical phone support. PATIENT INFORMATION PRIVACY AND PROTECTION In accordance with Appendix A, Handbook 6500.6 Checklist blocks 6, the C&A requirements do not apply to this requirement, and a Security Accreditation Package is not required. In reference to no. 7 there is no information to be protected. The equipment does not store any PHI/PII/PI, nor are there any hard drives/storage devices to service or remove. NURSE CALL Beds shall interface with available Nurse Call systems, which vary by facility. The following is a list of systems currently in use at the subject facilities. All associated cables must be provided for the appropriate system. TECH TONE Hill-Rom NMC 5.0 Rauland Response Rauland R4 Hill-Rom Rauland Responder V Westcom Jeron Dukane Rauland Borg Executone Ektacom Rauland-Borg Responder 5 Rauland Responder 4 Rauland Responder Navicare NOTE: THIS NOTICE WAS NOT POSTED TO FEDBIZOPPS ON THE DATE INDICATED IN THE NOTICE ITSELF (23-MAY-2019); HOWEVER, IT DID APPEAR IN THE FEDBIZOPPS FTP FEED ON THIS DATE. PLEASE CONTACT 877-472-3779 or fbo.support@gsa.gov REGARDING THIS ISSUE.
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