You already have items in your cart. Please view your cart to make changes to your existing cart.
Check your e-mail
We've sent a link to to reset your password.
The products and services listed in the quotation are offered by Philips Healthcare, a division of Philips Electronics North America Corporation (Philips) only under the terms and conditions described below.
back to top(a) Customer Responsibility. Customer shall be responsible, at its expense, for rigging, the removal of partitions or other obstacles, installation of safety switch or breaker, and restoration work. The products will be installed during normal working hours. Except where Philips has agreed in writing to provide construction services for a fee pursuant to a construction agreement and scope of work signed by Customer, Customer shall be responsible, at its expense, for the preparation of the installation site where the product will be installed including any required structural alterations.
Customer shall provide any and all plumbing, carpentry work, conduit, wiring including communications and/or computer wiring, network equipment, power supply, surge suppression and power conditioning (except to the extent they are expressly included in the quotation), fire protection and environmental controls, ground fault and isolation system, and other fixtures and utilities required to properly attach, install, and use the product.
Site preparation shall be in compliance with all safety, electrical, and building codes relevant to the product and its installation and use. The sufficiency of any installation site plans shall be the responsibility of Customer. Customer, at its expense, shall obtain all permits and licenses required by federal, state, or local authorities in connection with the installation and operation of the product, including any certificate of need and zoning variances.
(b) Customer shall advise Philips of site conditions at or near the location where equipment is installed five (5) days prior to the mutually agreed upon delivery date. The update shall include but not limited to the following: (i) Hazardous Materials. Asbestos and other hazardous materials, that could adversely affect the installation or pose a health or safety risk to Philips' personnel, and shall ensure that those conditions are corrected and hazardous materials removed, and that the site is fully prepared and available to Philips before installation work begins.
Customer represents and warrants that an asbestos survey of the facility has been performed to determine the presence, location, quantity and condition of asbestos containing materials (ACM) or presumed asbestos containing materials (PACM) at the facility; and the facility and/or work area does not contain any ACM or PACM or the facility and/or work area contains ACM or PACM, such material has been encapsulated or enclosed and the work will not disturb any such materials.(ii) Construction. All construction work in technical and operator room(s) is finished including but not limited to the responsibilities identified in 8.2 (a).
(c) Delays. If site preparation is not on schedule five (5) days prior to the mutually agreed upon delivery date, Philips and Customer will conduct an evaluation of the site and establish a revised installation schedule. In the event that installation is delayed by Customer within five (5) days prior to the mutually agreed upon delivery date or after the start of installation, Customer will be responsible for:
(i) storage and fees for the preservation and life support of the equipment to ensure high quality and long life of system(s); and, (ii) Costs associated with rescheduling and coordination for all resources and third party providers, including travel costs for split delivery and installation directly related to the delay in installation. If during installation Philips discovers hazardous materials (i.e. asbestos, etc.) all installation activities will stop and Customer will remove and dispose of the hazardous materials.
Once the issue giving rise to the delay has been rectified and the site meets the criteria set forth in this Section 8, Philips and Customer will conduct an evaluation of the site and establish a new installation schedule.
(d) Philips Responsibility. Unless additional professional services are purchased separately (including turnkey) and/or professional services are set forth in a statement of work or project implementation plan under the agreement for the product purchased hereunder, Philips role upon delivery will solely be to unpack the product, construct applicable pads (if required for certain products), connect the product to a safety switch or breaker to be installed by the Customer, and calibrate and test the product.
back to top
(a) THIRD PARTY CLAIMS FOR BODILY INJURY OR DEATH CAUSED BY PHILIPS' NEGLIGENCE OR PROVEN PRODUCT DEFECT;
(b) CLAIMS OF TANGIBLE PROPERTY DAMAGE REPRESENTING THE ACTUAL COST TO REPAIR OR REPLACE PHYSICAL PROPERTY DAMAGE;
(c) OUT OF POCKET COSTS INCURRED BY CUSTOMER TO PROVIDE PATIENT NOTIFICATIONS, REQUIRED BY LAW, TO THE EXENT SUCH NOTICES ARE CAUSED BY PHILIPS UNAUTHORIZED DISCLOSURE OF PHI; and,
(d) FINES/PENALTIES LEVIED AGAINST CUSTOMER BY GOVERNMENT AGENCIES CITING PHILIPS UNATHORIZED DISCLOSURE OF PHI AS THE BASIS OF THE FINE/PENALTY, ANY SUCH FINES OR PENALTIES SHALL CONSTITUTE DIRECT DAMAGES.
(a) Schedule 1: Imaging Systems Portfolio (IS);
(b) Schedule 2: Ultrasound Systems Portfolio (UL);
(c) Schedule 3: Cardiology Informatics Portfolio (CAI);
(d) Schedule 4: Patient Care and Monitoring Solutions Portfolio (PCMS);
(e) Schedule 5: Emergency Care & Resuscitation Portfolio (ECR);
(f) Schedule 6: Medical Supplies Portfolio (MS);
(g) Schedule 7: Enterprise Informatics Imaging (EII) Portfolio; and (h) Schedule 8: Invivo Corporation Portfolio (Invivo) (Products).
Schedule 1
Product Category | Products |
Interventional Guided Technologies (IGIT)� | Interventional X-Ray (iXR) |
Mobile C-Arms (Surg) | |
Multi Diagnost Eleva (MDE) | |
Cardio Vascular Systems | |
Volcano (IGT Devices) | |
Imaging Clinical Applications (ICAP) | IntelliSpace Portal (ISP) |
Diagnostic Imaging | Digital Radiography (DR) |
Mobile Radiography (MDR) | |
Radiography and Fluoroscopy (RF) | |
Women's Healthcare (WHC) Mammography Products | |
Computed Tomography (CT), | |
Magnetic Resonance (MR) | |
Invivo Coils | |
Positron Emission Tomography (PET/CT) | |
Advanced Molecular Imaging (SPECT & SPECT/CT) | |
Radiation Oncology (PROS) |
back to top
(a) 10% of the purchase price shall be due with Customer's submission of its purchase order.
(b) 70% of the purchase price shall be due on delivery of the major components of the product. Product installation will not begin until Customer has paid this portion of the purchase price.
(c) 20% of the purchase price shall be due when the product is available for first patient use. Available for first patient use means the product has been installed and substantially meets Philips' published specifications.
back to top
back to top
Required Details include: (a) Architectural drawing or sketch with complete dimensions including lengths, bending radii, bending angles, and pipe diameters for entire Helium Exhaust Pipe run from RF enclosure to discharge location. (b) Completed Helium Exhaust Pipe Verification Checklist (Provided by Local Philips Project Manager) (c) Picture showing the area where the Helium Exhaust Pipe will discharge.
Schedule 2
Product Category | Products |
Ultrasound Systems (UL) | Cardiovascular Ultrasound (CV UL) |
GeneralImaging Ultrasound Systems (GI UL) | |
Women's Health Care (WHC UL) |
back to top
(a) 100% of the purchase price shall be due thirty (30) days from Philips' invoice date.
back to top
Schedule 3
Product Category | Products |
Cardiology Informatics (CAI) Products | Image & Information Management System (Xcelera, Cardiology Enterprise Viewer) |
Hemodynamics (Xper IM, Xper Flex Cardio) | |
IntelliSpace Cardiovascular (ISCV)� | |
EKG Information Management (TraceMasterVue, IntelliSpace ECG) | |
Stress Testing System (ST80i) | |
Holter Monitoring System (DigiTrak) | |
Cardiographs (PageWriter) | |
IntelliBridge Enterprise Licensed Software (IBE) |
back to top
back to top
back to top
back to top
(a) Xper IM, Xper Flex Cardio, TraceMasterVue, IntelliSpace ECG, Xcelera Cardiology Enterprise Viewer IntelliSpace Cardiovascular (ISCV), and IntelliBridge Enterprise Licensed Software (IBE). . For a period of ninety (90) days from the date that a Licensed Software Upgrade is available for first patient use, Philips warrants that such Licensed Software Upgrade shall substantially conform to its documentation. Licensed Software Upgrades do not include hardware costs.
(b) Xper IM, Xper Flex Cardio, TraceMasterVue, IntelliSpace ECG, Xcelera Cardiology Enterprise Viewer IntelliSpace Cardiovascular (ISCV), and IntelliBridge Enterprise Licensed Software (IBE). Philips warrants that any Philips-provided hardware purchased with the exception of patient cables and/or disposable items (which have no warranty), shall be free from material defects in material and workmanship under normal use and service for a period for a period of 12 months beginning the date available for first patient use.
back to top
back to top
back to top
back to top
back to top
back to top
back to top
back to top
back to top
back to top
back to top
back to top
back to top
back to top
Philips standard migration tool set-up service (Migration Tool Set-Up Service) consists of Philips installing a migration solution tool, configuring the migration interface, testing the migration solution tool, and training the Customer to operate and manage the migration tool for Customer to perform the data migration (Migration Set-up Tool Activities). For the purposes of clarification, Migration Set-Up Activities do not include Philips performing the migration, including starting and stopping the migration tool process, loading off-line media, monitoring the process, and correcting the migrated data.
Unless Customer purchases a separate data migration project management consulting service from Philips and signs an SOW clearly indicating that Philips will be performing and managing the data migration on the Customers behalf (Data Migration Project Management Consulting Service), Philips is responsible solely to perform the Migration Set-Up Activities.
In all instances, Philips shall have no responsibility under either its Migration Tool Set-Up Service or Data Migration Project Management Consulting Service to: (a) locate missing studies; (b) fix corrupt media or studies; or, (c) repair failed Customer legacy hardware discovered during the migration service. Philips shall have no responsibility under the migration services to migrate studies affected by the foregoing events. Additionally, Customer shall have the sole responsibility to estimate the number of studies required to be migrated and to pay any additional costs that result from an inaccurate estimate.
Schedule 4
Product | Category |
Measurement and Monitors | IntelliVue Patient Monitors and Systems |
IntelliVue Telemetry System | |
Fetal Monitors | |
Ventilators | |
Suresigns and VM Series Family of monitors | |
Clinical measurements | |
IntelliSave | |
Invivo Monitors | |
Clinical Informatics | IntelliVue Critical Care and Anesthesia |
CompuRecord� | |
IntelliSpacePerinatal | |
IntelliSpace ECG | |
IntelliSpace Event Management (IEM) | |
IntelliVue Guardian Systems | |
IntelliBridge Enterprise |
back to top
back to top
back to top
back to top
back to top
back to top
The Philips IntelliVue Information Center is a secondary vital signs monitoring tool that is used by Customers to monitor the activity arising from alarms that sound from a Vital Signs Patient Care Monitor at the patient bedside. Philips advises that the likelihood of power or bandwidth outages is generally greater when using a medical device on a general network vs. a network dedicated solely to its use.
In the event a power or bandwidth outage were to directly affect the Philips IntelliVue Information Center's ability to communicate with a bedside Vital Signs Patient Care Monitor, the Philips IntelliVue Information Center would not be available to get real time alarm information from a bedside Vital Signs Patient Care Monitor. Accordingly, Customer is reminded that its nursing protocols at the patient room floor must be based on using the Philips bedside Vital Signs Patient Care Monitor, at all times, as the primary medical device to use and respond to, for monitoring patient's vital signs at the patient bedside.
back to top
back to top
back to top
It is the customers' responsibility to deploy applicable updates at their discretion. Learn more at http://www.healthcare.philips.com/us_en/support/productsecurity/ Security for Clinical Networks (Part Number 4535 643 73021) for additional security related information.
back to top
back to top
back to top
back to top
Schedule 6
| Product Category | Products Consumables and Sensors (non serialized) |
Patient Care | Fetal & Medical Supplies and Consumables (MCS) | Accessories� / Supplemental |
ECG Cables and Lead sets | ||
ECG Electrodes | ||
Fetal Measurements | ||
Gas Measurements | ||
NIBP Cuffs | ||
Paper | ||
SpO2 Sensors | ||
Temperature Probes | ||
Emergency Care & Resuscitation | AED Consumables | |
ALS Consumables | ||
Hospital Respiratory Care | Masks | |
Children's Medical Ventures | Jaundice | |
Safety and Feeding | ||
Invivo | Invivo Monitor Consumables |
back to top
back to top
(a) through Philips Healthcare eStore,(http://www.philips.com/newhealthcarestore .);
(b) via EDI; or
(c) a Philips authorized distributors.
Please call 800-225-0230 to obtain a list of authorized distributors and/or EDI information.back to top
back to top
back to top
Schedule 7
Product Category | Products |
Enterprise Imaging Informatics (EII) | IntelliSpace PACS |
MammoDiagnost VU Mammography workstation |
back to top
back to top
To the extent there is a conflict, the order of priority for IntelliSpace PACS purchases is:
1st Priority - IntelliSpace PACS Services Attachment
2nd Priority - Schedule 7
3rd Priority - Terms and Conditions of Sale
back to top
Schedule 8
Product Category |
| Products |
Magnetic Resonance Imaging (MRI) Coils | Capital Coils |
|
Consumables | Consumables Coils |
|
back to top
back to top
back to top
Returns will be subject to a 15% restocking fee.
back to top
STANDARD PRODUCT WARRANTY PERIODS
back to top