Pre-Bid Conference
Known from stored extractionA specific pre-bid conference is identified in the procurement notice.
This means the requirement is present in the stored extraction. It does not mean your company satisfies it.
Buying agencyPHILIPPINE HEART CENTER
Bid Brief
Stored notice data. Confirm all decisions with the official documents.
The stored deadline is approaching. Confirm the official deadline before investing more time.
Use the supporting sections below to verify the evidence.
Compare stored requirements with evidence from this browser. Unknown answers stay as Needs verification.
Checking the stored deadline…
Add only the evidence relevant to this bid, or screen with unknown answers.
Not assessed yet
Stored category: Hospital / Medical Equipment Services
1 Description of Function: 1.1. The Holter monitor system with 3 recorders is a type of portable electrocardiogram (ECG). It records the electrical activity of the heart continuously over 24 hours or longer while you are away from the doctor's office. A standard or "resting" ECG is one of the simplest and fastest tests used to evaluate the heart. 2 Operational Requirements 2.1. System complete with all accessories as specified in the Technical Specifications below. 3 Technical Specifications 3.1.1. Holter Software System/ Algorithms 3.1.2 Dicom compliant 3.1.3. Prepare recorder with patient data, import recording, delete recording Multilevel template 3.1.4. Rhythm Analysis 3.1.5. HRV Tabular and trend analysis 3.1.6. ST Tabular and trend analysis 3.1.7. Pacemaker Detection Feature 3.1.8. QT, Qtc Measurement/analysis 3.1.9. Ability to correct/reject artifact Software Features 3.2.1. Customizable Interface-capability to easily add/delete/edit features without tech support. 3.2.2. Able to provide summary in Statistics in Tabular and Trend form, histograms, Rate and Rhythm Diagnostics (arrhythmia density, frequency, duration) including atrial fibrillation burden, Qtcc, ST segment, HRV 3.2.3 Local database 1,000 tests lower limit 3.2.4. Rhythm analysis – Atrial fibrillation and atrial flutter, pacemaker detection 3.2.5.Easy identification of abnormal beats and ability to edit machine derived notations. Manual or auto-adjust ECG sensitivity features 3.2.6. Customizable printing function – how many and which channels/leads to print 3.2.7. Recorder 3.3.1 On screen lead map display to ensure proper lead placement and ensure artifact-free hook-up 3.3.2 .Individual lead check/lead off detector 3.3.3. Can do 3 channel and 12 channel 3.3.4. Fast Download 3.3.5. Patient’s activity registration. Indication of patient’s activity: walking, running, stopping 3.3.6. Capability of up to 7 days recording 3.3.7. Recorder display: 2.2” TFT Color display, 4-way joystick navigation button for easy navigation comments while preparing the patient, capable of recording events by means of central button at least IP 4X 3.2.8 Include 5 wire cable for 3 channel and 10 wire cable for 12 channel ECG Channel 3.4.1 Capable of 3-12 channel display 4 System Configuration Accessories, spares and consumables Workstation 4.1.1 CPU 4.1.1a Processor: Intel Core i7 4.1.1b Operating system at least Microsoft Windows 10 or higher 4.1.1c Minimum Graphics: 1024 x 768 4.1.1d RAM: 16GB at least 4.1.1e Network Interface: 10/100/1000 4.1.1f Hard Drive capacity: 1TB at least 4.1.1g Archive: CD-RW, DVD-R, DVD-RW, Network drive 4.1.1h USB: 2.0 or greater 4.1.1i CD ROM: 32 x Drive 4.1.1j Video: Any Direct Draw-capable video card capable of 1024 x768 with 65K (16-bit) colors 4.1.2 Monitor 4.1.2a Monitor Size: at least 27 inches 4.1.2b Type: High resolution, Super VGA color 4.1.2c Resolution: 16-bit minimum, 1024 horizontal x 768 vertical 4.1.3 Laser Jet Printer 4.1.3a Print resolution: 1200 x 1200 dpi 4.1.3b Printing speed: at least 30 page/min, color printer Additional 5 pcs patient cable
5.1. The unit shall be capable of being stored continuously in ambient temperature of 0-50°C and relative humidity of 15-90% 5.2. he unit shall be capable of operating in ambient temperature of 20-30°C and relative humidity of less than 70%. 5.3T. The equipment shall comply with the requirements of IEC 60601-1-2:2014 on electromagnetic compatibility (EMC) for medical electrical equipment. 6 Power Supply 6.1. Power adapter AC input: 100-240 VAC, 50/60Hz fitted with PHC electrical outlet. 6.2. Resettable over-current breaker shall be fitted for protection 6.3. UPS with minimum one-hour back-up should be supplied with the system 7 Standards, Safety and Training 7.1. Manufactures/Supplier should have a valid ISO 9001 certification 7.2 The medical equipment should have an ISO 13485 certification to ensure quality management standard for medical devices 7.3. Product must be CE, UL, BIS or regional certification 7.4. Authorized Distributor/Supplier should be a Philippine FDA Certified and License to operate 7.5. In the event that a Philippine FDA Certificate of Product Registration (CPR) is not yet available, the supplier may submit a valid and applicable Certificate of Medical Device Notification (CMDN) or Certificate of Medical Device Registration (CMDR), as appropriate. 7.6. Comprehensive warranty for two (2) years parts and service, inclusive of quarterly preventive maintenance and calibration. 8 Documentation 8.1. User/Technical/Maintenance manuals to be supplied in English. 8.2. Certificate of calibration and inspection. 8.3. List of important spare parts and accessories with their part number and costing. 8.4. List of Equipments available for providing calibration and routine maintenance support as per manufacturer documentation in service / technical manual 9 Others 9.1 Delivery period – 90 calendar days. Pre-bid Conference Date Time Venue 22/10/2026 10:00 AM Philippine Heart Center East Avenue, Quezon City Old Chapel, Hospital Bldg., PHC Other Information Description ABC
Created by Rachelle Henson Cortez Date Created 12/10/2026 The PhilGEPS team is not responsible for any typographical errors or misinformation presented in the system. PhilGEPS only displays information provided for by its clients, and any queries regarding the postings should be directed to the contact person/s of the concerned party. © 2004-2026 DBM Procurement Service. All rights reserved. Help | Contact Us | Sitemap
This presentation only restructures stored source text. It does not add quantities, specifications, or delivery terms.
These checks organize what BidAssistant found. “Known from stored extraction” describes the source record, not your company’s eligibility. Unknowns remain verification items.
A specific pre-bid conference is identified in the procurement notice.
This means the requirement is present in the stored extraction. It does not mean your company satisfies it.
Oct 13, 2026, 12:00 AM
Nov 5, 2026, 10:00 AM
5 days leftOct 13, 2026, 3:58 AM
Oct 13, 2026, 3:58 AM
These are stored timestamps. A missing pre-bid or other procurement date is not shown.
Open the stored PhilGEPS source link
Freshness: First saved / captured Oct 13, 2026, 3:58 AM; last database update Oct 13, 2026, 3:58 AM.
New notices are collected periodically, but this service does not routinely refresh already-known notices. Stored dates and status may miss deadline extensions, cancellations, or amendments. Always check the latest official PhilGEPS notice. First-saved and last-update times describe our stored record, not a fresh check of the official notice.
BidAssistant PH is an independent discovery and screening aid, not PhilGEPS or a procuring agency.