IKLAN PEROLEHAN TERUS HOSPITAL PENGAJAR UNIVERSITI PUTRA MALAYSIA
IKLAN PEROLEHAN TERUS HOSPITAL PENGAJAR UNIVERSITI PUTRA MALAYSIA
ASSALAMUALAIKUM WBT & SALAM SEJAHTERA,
Dipelawa dari kalangan pembekal yang berminat untuk menyertai tawaran sebutharga berikut :
TAJUK SEBUTHARGA | : | MEMBEKAL, MENGHANTAR, MENGUJI DAN MENTAULIAH COMPLEX PATIENT MONITOR, HOSPITAL PENGAJAR, UNIVERSITI PUTRA MALAYSIA |
TARIKH TUTUP | : | 31 OKTOBER 2020 @ 4.30 PETANG |
SPESIFIKASI | : | SEPERTI LAMPIRAN |
CARA MENGHANTAR SEBUTHARGA | : | EMEL/SERAH TANGAN KEPADA MAKLUMAT SEPERTI DIBAWAH |
PEMOHON | : | XXXXXXX XXXXX XXXXX |
EMEL | : | |
NO. TELEFON | : | 00-0000 0000 |
ALAMAT SERAH TANGAN | : | UNIT KECEMASAN STROK RESQ, HOSPITAL PENGAJAR, UNIVERSITI PUTRA MALAYSIA |
Sekian, terima kasih.
MEMBEKAL, MENGHANTAR, MENGUJI DAN MENTAULIAH COMPLEX PATIENT MONITOR, HOSPITAL PENGAJAR, UNIVERSITI PUTRA MALAYSIA
TAJUK:
BIL | ITEM | KUANTITI |
1. | COMPLEX PATIENT MONITOR Specification: 1. The patient monitor is used for monitoring the physiological parameters of patients (Adult, Pediatric, Neonatal). 2. Capable for monitoring: 2.1. ECG 2.2. Oxygen saturation 2.3. Perfusion index 2.4. Heart rate 2.5. Respiraton rate 2.6. Temperature 3. Physical specification: 3.1. Minimum of 4 hours of working time with internal Li-ion Battery. 3.2. Weight ≤3.5kg, inclusive of Standard parameters configuration, a lithium battery. 3.3. Fanless design - reduces noise power consumption. 3.4. The monitor must have 0.75m drop- protection and IPX1 water resistance. 4. Display screen: 4.1. Screen 10” color LED with resolution 800x600 pixels 4.2. Minimum 7 waveform channels. 4.3. Capable of multiple on-screen display modes. 5. Data storage and review: 5.1. Max. 48 hrs full disclosure waveforms, NIBP: 1600 measurements. 5.2. Trend data: 1200hrs. 5.3. 1800 events and associated waveforms. 5.4. Able to review Discharged patient data such as trends and events. 5.5. The monitor shall able to view at least 10 other patient monitors that are connected to the same LAN network. | 5 |
5.6. Optional internal storage/ external USB storage, supports power-down storage and data transferring via USB drive. 5.7. The monitor shall meet IEC60601-1 safety specifications. 6. Parameters: 6.1. Electrocardiogram 6.1.1. Capable of 3 and 5 lead ECG monitoring. 6.1.2. ECG should have automatic lead fall back, adjusting the monitoring to suit available leads. 6.1.3. Capable up to 24 classifications of arrhythmias analysis for adult, pediatric and neonate. 6.1.4. The monitor shall be able to provide users with an analysis of heart rate changes and distribution over the last 24 hours. This report must be able to be printed out. 6.1.5. The monitor must be able to analyze ST segments for individual leads and display them on the screen. Measurement range: -2.0mV to +2.0mV. 6.1.6. Users shall be able to save at least 15 ST reference segment groups. 6.1.7. The ST-point position shall be able to be adjusted relative to the J-point at either [J+60/80ms], [J+40ms], [J+60ms] or [J+80ms]. 6.1.8. The monitor shall be capable of QT/QTc interval monitoring on all ECG leads, and users shall be able to choose between 4 different correction formulas for calculation, ie. Xxxxxx, Bazett, Xxxxxxxxxx and Framingham. 6.2. Respiration 6.2.1. Technique: Trans-thoracic impedance. 6.2.2. Resolution:1rpm Accuracy: 7to 150 rpm: ±2 rpm or ±2%, whichever is greater. 6.3. Non-invasive blood pressure 6.3.1. Technique: Oscillometric. 6.3.2. Operation mode: Manual, Automatic interval, STAT, Sequence. |
6.3.3. User shall be able to set custom intervals for NIBP measurement, up to 5 different periods. 6.3.4. The monitor shall be able to provide users with an analysis of NIBP changes and distribution over the last 24 hours. This report must be able to be printed out. 6.4. Oxygen saturation (SpO2) 6.4.1. Refreshing rate: ≤2 s. 6.4.2. Accuracy: ±2% (70-100%, Adult/Ped), ±3% (70-100%, Neo) , Unspecified (0-69%). 6.4.3. The monitor shall be able to measure Perfusion Index. 6.5. Temperature 6.5.1. Measurement range from -1 to 45 degree Celsius 7. Alarm system 7.1. Clear audible and visual alarms for all monitored parameters. 7.2. Users shall be able to configure and set criteria to trigger an event alarm. 7.3. When the set alarm limit is exceeded, it shall trigger alarm tones according to the severity of clinical situation, classified into at least three categories: high level, medium level and low level, along with alarm messages. 7.4. The monitor shall have temporary alarm suppression. 7.5. The monitor shall be able to automatically adjust alarm limits based on patient’s measured values. 8. System function 8.1. Support Hemodynamic and dose calculations. 8.2. The user shall able to configure graphical menu keys for fast access to commonly used functions. 9. Accessories (Each monitor must come with the following accessories): 9.1 NIBP Tubing, Adult, Peds, Neonate, with air plug connectors (3m)ECG x 1 unit |
9.2 Reusable NIBP cuff 4sizes: Adult, Large Adult, Child, Neo x 1 each 9.3 Reusable SpO2 Adult, Peds and Neo x 1 each 9.4 SpO2 Cable x 1 unit 9.5 Temperature Skin Probe Adult x 1 unit 9.6 Electrode+cable+wires: 3-lead x 1 set 10. Trolley 10.1 Trolley with basket for 4 unit of complex patient monitor. 11. Wall-mounted bracket 11.1 Wall-mounted bracket for 1 unit of complex patient monitor. 12. Documentation 12.1 The system shall come supplied with its original instruction manual or any other system-related information or documentation and a quick start guide. 13. Installation & Commissioning 13.1 On-site installation and commissioning must be performed by qualified and trained service engineer after delivery. 14. User training 14.1 Training for system and software must be performed on-site by trained technical support personnel. 14.2 Training must include basic theory, application (function & operation), troubleshooting and maintenance. 15. After sales support 15.1 List of technical support personnel must be provided. 16. Warranty 16.1 The product must have minimum two (2) year warranty against manufacturing defects, parts, labour and software. 17. Special Hospital Requirements: 17.1 All equipment supplied to the Hospital Pengajar UPM shall conform to relevant international/national electrical safety standard; |
17.1.1 MS IEC 60601-1 for medical electrical equipment. 17.1.2 MS IEC 61010-1 for laboratory equipment; and relevant product standards (if any). 17.2 The medical equipment to be procured shall comply with Malaysian power supply rating of 240 V with a tolerance of +10 % -5 %, 50 Hz (single phase) and 415 V with a tolerance of +10 % -5 %, 50 Hz (three-phase). 17.3 The condition for purchase shall include provision for future modification of equipment and provision for software upgrades. 17.4 The criteria for selection shall be based on efficacy, effectiveness, performance, safety, reliability, features, ease of use, cost-effectiveness, service, training and continuous support for the user and equipment maintenance. 17.5 Supplier shall provide complete copies of the following items to the Hospital Pengajar UPM : 17.5.1 user manual; 17.5.2 service or maintenance manuals; 17.5.3 circuit diagrams and drawings (if any); 17.5.4 relevant software inclusive of access codes (if any); 17.5.5 parts list; 17.5.6 PPM checklist according to manufacturer recommendation; and 17.5.7 other necessary documents/items. 17.6 Supplier shall provide complete technical training to the Biomedical Engineering Services and user training. 17.7 Final payment shall be paid to the supplier upon meeting the terms and conditions of contract/purchase order and clearance from Biomedical Engineering Services. |
MAKLUMAT PEMOHON : | XXXXXXX XXXXX XXXXX PENOLONG PEGAWAI PERUBATAN 00-0000 0000 |
EMEL : | x_xxxxxxxxxx@xxx.xxx.xx DAN xxx.xxxxx@xxx.xxx.xx (Pembekal yang tidak cc Sebutharga ke Pengarah HPUPM boleh menyebabkan sebutharga anda tidak diterima) |