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 TRANSPORT PATIENT MONITOR, HOSPITAL PENGAJAR, UNIVERSITI PUTRA MALAYSIA
TARIKH TUTUP	:	2 NOVEMBER 2020 @ 4.30 PETANG
SPESIFIKASI	:	SEPERTI LAMPIRAN
CARA MENGHANTAR SEBUTHARGA	:	EMEL/SERAH TANGAN KEPADA MAKLUMAT SEPERTI DIBAWAH
PEMOHON	:	XXXXXXX XXXXX XXXXX
EMEL	:	x_xxxxxxxxxx@xxx.xxx.xx DAN xxx.xxxxx@xxx.xxx.xx
NO. TELEFON	:	00-0000 0000
ALAMAT SERAH TANGAN	:	UNIT KECEMASAN STROK RESQ, HOSPITAL PENGAJAR, UNIVERSITI PUTRA MALAYSIA

Sekian, terima kasih.

TAJUK: MEMBEKAL, MENGHANTAR, MENGUJI DAN MENTAULIAH TRANSPORT PATIENT MONITOR, HOSPITAL PENGAJAR, UNIVERSITI PUTRA MALAYSIA

BIL	ITEM	KUANTITI
1.	TRANSPORT PATIENT MONITOR Description: 1. The monitor is suitable for all types of patients which are adult, paediatric, infant, and neonate. 2. Display requirements: 2.1. LCD Colour Display with Adjustable Brightness 2.2. Touchscreen 2.3. Automatic screen rotation provides upright display for vertical or horizontal monitoring positioning. 2.4. Parameters- Numerical Display of Spo2, Pulse Rate & Perfusion Index 2.5. Variable Pleth Waveform 2.6. Trend display up to 96 hours at 2 seconds sampling rate 2.7. Access to Menu and user settings for configuring and managing alarms 3. Display range: 3.1 Oxygen Saturation ( SpO2)- 0 – 100% 3.2 Pulse Rate(PR) - 25-240bpm 3.3 Perfusion Index(PI) - 0.02-20% 4. Saturation accuracy: 4.1 Saturation Range : 60% to 80% 4.1.1 Accuracy when there is no motion for Adults/ Infants/Pediatrics : 3% 4.2 Saturation Range : 70% to 100% 4.3 Accuracy when there is no motion for Adults/ Infants/Pediatrics : 2% and Neonates: 3% 4.4 Accuracy when there is motion for Adults/ Infants/Pediatrics/Neonates : 3% 4.5 Accuracy when there is Low Perfusion for Adults/ Infants/Pediatrics/Neonates : 2% 5. Pulse rate accuracy: 5.1 Averaging modes : 2, 4, 8, 10, 12, 14 or 16 seconds 5.2 Sensitivity : APOD, Normal and Max	2

6. Non-invasive blood pressure:

6.1 Measurement Accuracy: Between 0 mmHg and 300 mmHg (± 3mmHg)

6.2 NIPB Display Ranges: Adult, Pediatric, Neonatal

6.3 Systolic: 40-260 mmHg(Adult), 40-230 mmHg(Pediatric), 40-130 mmHg(Neonatal).

6.4 Diastolic: 20-200 mmHg(Adult), 20-160 mmHg (Pediatric), 20-100 mmHg(Neonatal).

6.5 MAP: 26-220 mmHg(Adult), 26-183

mmHg(Pediatric), 26-100 mmHg(Neonatal).

7. Technical requirements:

7.1 Should have Signal Extraction Technology

7.2 Should generate audible pulse tone during motion and low perfusion

7.3 Should be upgradable to measure optional PVI (Pleth variability Index)

7.4 Should display SpO2, Pulse Rate and perfusion Index readings during motion and low perfusion

7.5 Should have provision for Desaturation Index and 3D alarms.

7.6 Should be upgradeable

7.7 Should be able to perform screen capture to record the current screen with readings.

7.8 Communication and Connectivity via Bluetooth, Wi-fi and Ethernet.

8. Alarms:

8.1 Audible and visual alarms for High/Low SpO2, High/Low Pulse Rate, probe off, cable disconnects and low battery.

9. Battery requirements:

9.1 Rechargeable Batteries

9.2 Capacity – 4 hours

10. Physical characteristic:

10.1 Should be less than 1.2 kg

11. Alarm:

11.1 Operating Temperature: 0-35 °C

11.2 Operating Humidity: 10-95%

11.3 Atmospheric Pressure: 540-1,060 mBar

12. Regulatory requirements:

12.1 FDA approved product

12.2 Manufacturer/Supplier should have ISO certification for quality standards

13. Compliance requirements:

13.1 Safety Standards: ANSI/AAMI ES 60601-1, CAN/CSA C22.2 No. 60601-1, IEC/EN 60601-1, 3rd Ed.

13.2 Pulse Oximeter Standards: ISO 80601- 2-61

13.3 Alarm Standards: IEC 00000-0-0

13.4 EMC Standards: EN 00000-0-0, Class B

13.5 Degree of Protection: TypeBF, DefibProof- Applied Part

14. Essential components and accessories:

13.1 Main device (1 unit)

13.2 AC power cord (1 unit)

13.3 SpO2 adapter cable adult (1 unit)

13.4 SpO2 adapter cable paeds (1 unit)

13.5 SpO2 adapter cable neonate (1 unit)

13.6 Connector patient cable 12 feet (1 box)

13.7 Adult reusable sensor 3 feet (1 box)

13.8 NIBP patient hose 3 meters, male (1 unit)

13.9 NIBP patient hose 3 meters, female (1 unit)

13.10Reusable NIBP cuff adult (1 unit) 13.11Reusable NIBP cuff adult large size (1

unit)

13.12Reusable NIBP cuff paeds (1 unit) 13.13Reusable NIBP cuff neonate (1 unit) 13.14Reusable adult sensor (1 unit) 13.15Reusable paeds sensor (1 unit) 13.16Reusable wrap multisite neonate sensor

(1 unit)

13.17Disposable foam wrap neonate sensor (3 pcs)

13.18Disposable neonate cuff size 2 (5 pcs) 13.19Disposable neonate cuff size 3 (5 pcs) 13.20Disposable neonate cuff size 4 (5 pcs) 13.21Operation instruction

15. 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.

16. After sales support

15.1 List of technical support personnel must be provided.

17. Warranty

16.1 The product must have minimum two (2) year warranty against manufacturing defects, parts, labor and software.

18. Service

17.1 Free comprehensive maintenance service 2 times during the warranty period

19. Special Hospital Requirements:

18.1 All equipment supplied to the Hospital Pengajar UPM shall conform to relevant international/national electrical safety standard:

18.1.1 MS IEC 60601-1 for medical electrical equipment.

18.1.2 MS IEC 61010-1 for laboratory equipment; and relevant product standards (if any).

18.2 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).

18.3 The condition for purchase shall include provision for future modification of equipment and provision for software upgrades.

18.4 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.

18.5 Supplier shall provide complete copies of the following items to the Hospital Pengajar UPM:

18.5.1 user manual;

18.5.2 service or maintenance manuals;

18.5.3 circuit diagrams and drawings (if any);

18.5.4 relevant software inclusive of access codes (if any);

18.5.5 parts list;

18.5.6 PPM checklist according to manufacturer recommendation; and

18.5.7 other necessary documents/items.

18.6 Supplier shall provide complete technical training to the Biomedical Engineering Services and user training.

18.7 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)