ITB No.065.26- 3 units Intra Aortic Balloon Pump (IABP) Machine

ITB No.065.26- 3 units Intra Aortic Balloon Pump (IABP) Machine 1. Description of Function The machine provides temporary mechanical support to heart through a process called counterpulsation based on the precise timing of balloon inflation and deflation relative to the patient's heartbeat, improving blood flow and reduce the cardiac workload. 2 Operational Requirements System complete with all accessories as specified in the Technical Specifications below. 3. Technical Specifications 3.1 General Specifications: 3.1.1 The machine must be able to accept fiber-optic and non-fiber optic catheters 3.1.2 Transportable, compact IABP system 3.1.3 Battery mode with minimum 90 minutes back-up 3.1.4 Display: 3.1.4a High definition LCD or LED color touch screen 3.1.4b Size: at least 10-14 inch diagonal display 3.1.4c 1024 x 768 pixel or higher 3.1.4d With ability to lock screen for patient safety 3.1.4e With ability to freeze patients data on screen 3.1.4f With detachable monitor 3.1.4g Automatically evaluates and select the best lead and trigger source but can be manually set 3.2 System modes: 3.2.1 Auto pilot mode or auto operation mode 3.2.1a Responds to changes in signal quality by automatically selecting new trigger source 3.2.2 Operator or Semi-Auto operation mode 3.3 Trigger Modes: 3.3.1 ECG 3.3.1a Pattern 3.3.1b Peak 3.3.1c Atrial Fibrillation 3.3.2 Pacer 3.3.2a Ventricular pacing 3.3.2b Atrial pacing 3.3.3 Arterial Pressure 3.3.4 Internal equivalent mode during systole 3.4 The following data must be available on the screen: 3.4.1 Patient hemodynamics: Heart rate, AP-systolic, diastolic, augmented and mean arterial pressure 3.4.2 ECG source, alarm status timer, “on battery” indication, operation mode selection, AP alarm parameter and limit, timing settings, helium tank level, arrhythmia detection (arrythmia can be seen/recognized in ECG waveform in the display), and timing status 3.4.3 Operation status: Operation mode, trigger mode, helium tank gauge, alarm/battery change status, balloon volume. 3.4.4 Help screen must be available on demand 3.4.5 The following parameters must be displayed in multi- color waveform: ECG, AP and Balloon volume 3.4.6 Operators must be able to measure arterial pressure and balloon waveform through a cursor or a reference line. 3.5 The machine must have a strip chart recorder 3.6 Pneumatics 3.6.1 Stepper motor/scroll compressor driven bellows using UPS-graded helium 3.7 Inflation/Deflation timing Methods: 3.7.1 Manual option for users to set inflation, depletion and operation mode. 4. System Configuration Accessories, spares and consumables 4.1 Twelve (12) Disposable or refillable helium Tank Cylinder 4.2 Six (6) pcs. 5-lead ECG Cable 4.3 Six (6) cable for arterial pressure transducer (compatible with hospital set up) 4.4 Three (3) Slave cable and adapter for ECG and arterial pressure (compatible with hospital set up monitor) 4.5 One (1) unit Intra-Aortic Balloon Pump Simulator 4.6 Fifteen (15) disposable Aterial Pressure Transducer 4.7 Twelve (12) Reusable Pressure Inflator 500ml 4.8 Three (3) unit Doppler Machine 5. Environmental factors 5.1 The unit shall be capable of being stored continuously in ambient temperature of 0-50deg C and relative humidity of 15-90% 5.2 The unit shall be capable of operating in ambient temperature of 20-30 deg C and relative humidity of less than 70% 5.3 Shall meet IEC-60601-1-2 :2014 (Or Equivalent BIS) General Requirements of Safety for Electromagnetic Compatibility or should comply with 89/366/EEC; EMC-directive. 6. Power Supply 6.1 Power input to be 110-240 voltage, 60Hz fitted with hospital electrical outlet 6.2 Back-up battery operating 90 to 180 minutes on full charge 7. Standards, Safety and Training 7.1 Manufactures/Supplier should have ISO 13485 certificate to Quality Standard. 7.2 Should be CE, UL or BIS approved product 7.3 Valid Certificate of Medical Device Registration from FDA Philippines 7.4 Comprehensive technical training for Hospital BIOMED and User’s training to staff for familiarity with the system. 7.5 Electrical safety conforms to standards for electrical safety IEC 60601-1 General Requirements (OR EQUIVALENT international/national standard) 7.6 The warranty period 5 years including parts 7.7 Machine manufacture and assembly date must not exceed 18 months 7.8 Periodic maintenance would be every 6 months during which maintenance parts needed to be replaced will still fall under warranty of 5 years. 7.9 Guarantee on availability of spare parts and consumables in the market for 10 years after machine acquisition 7.10 Fully functional loaner within 24 hours in the event of malfunction. 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 NOTE: You can view the complete bidding documents at our agency's website: [email protected] Pre-bid Conference Date Time Venue 29/10/2026 10:00 AM Philippine Heart Center East Avenue, Quezon City 5th Floor, Old Chapel, Hospital Bldg., PHC Other Information Description ABC 1. 3 units Intra Aortic Balloon Pump (IABP) Machine = P 21,000,000.00 Created by Rachelle Henson Cortez Date Created 14/10/2026 The PhilGEPS team is not responsible for any typographical errors or misinformation presented in the system. 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