# TECHNICAL PARAMETERS SPECIFIED RESULT

1 APPLICATION Adult and Pediatric & Neon. yes

2 PIPELINE GAS INLETS 3 (O2, N20,Air) yes
3 Pressure Indicator for all above gasses Either Gauge or Digital display electronic
4 GAS CYLINDER YOKES E size ( O2, 1 x 1 N2O) yes
5 Pressure Indicator for all above gasses. Either Gauge or Digital display electronic
6 FLOWMETER FOR O2 , N2O & AIR Yes, Electronic or Mechanical control
with digital display. yes

7 Oxygen range 0.25- 15 lit/min, 0.1 - 20

8 Nitrous oxide range 0-10 lit/min, yes
9 Compressed Air range 0-10 Lit/min, yes
10 Emergency O2 Yes , Semi closed yes
11 Pressure relieve valve Yes yes
12 ANAESTHETIC GAS SCAVENGING SYSTEM Should be either passive or active passive
according to the hospital gas system

13 CO2 Absorber complete, inclusive ventilator & Yes

absorber bypass. yes

14 DRAWER FOR UNIT WIDE & DEEP Yes, 2 1

15 SUCTION SYSTEM Yes, central or ventury yes
16 O2 FAIL-SAFE Yes yes
17 HYPOXIC MIXTURE FAIL-SAFE Yes yes
18 VAPORIZERS Yes, 2 1
19 Agents Sevoflurane, Isoflurane .key filler or
quick filler yes

20 Type Variable by pass/direct injection electronic injection

21 Number 2 VAPORIZERS 1
22 Interlock Yes
23 AUTOMATIC VENTILATOR Yes yes
24 Operated by compressed air and in case of Yes
emergency, capable to operate by compressed
oxygen yes

25 Screen Display and Size Yes, LCD, TFT 12 AND ABOVE 15, LED
26 Primary controls / Ventilation modes Volume control + SIMV mode of yes
ventilation pressure support / Pressure
Control specify mode of ventilation.

27 Tidal volume Range, mL 2 - 1500 ml or better 20-2000

28 100 ml/min- 15 L/min
29 Frequency, bpm 4-100 yes
30 Inspiratory flow, L/min 1-120 ( 80 max sustained) 200 l/min
31 Inspiratory pause 5-60 % yes
32 Pressure-limit, 6-80 cm H2O 0-80-120
33 PEEP, cm H2O 4 - 20 or better 0-50
34 MONITORS yes
35 Airway pressure Yes
36 Hi-pressure alarm YES
37 Sub-atmospheric Yes
38 pressure alarm Yes
39 Continuing pressure alarm. Yes
40 Low pressure/apnea Yes
41 Other press alarms Yes
42 Expiratory vol/flow Yes
43 Rate alarm Yes
44 Apnea alarm Yes
45 Reverse flow alarm Yes
46 High/low min vol Yes
47 High/low flow According to inspiratory flow
48 O2 concentration Specify , ( 21 % - 100 % )
49 Response time, Vol % Yes
50 Apnea alarm Yes
51 AN EASTHESIA PATIENT MONITOR Yes , modular Touch screen 17
52 Display screen / no.channell 17 approx .LCD , TFT 8 channel Touch
screen

53 Housing Module, SPECIFY

54 Measure parameter ECG/Resp. Heart Rate, SPO2, NIBP, 2
IBP, 2 Temp.. &
Anesthetic Gasses with FiO2, CO2
Capnograph. Bis or equivalent , ALL
PARAMETER NEEDED IN OR
OPRATION

55 N2O , EtCO2 & FiO2 Yes , numerical & graphic

56 Agent monitors All anesthetic agents
57 Type of agents 2 agent sevoflurane , isoflurane
,
58 Auto ID Yes
59 Agent conc alarm Yes
60 ECG 3-5 lead with resp. Yes
61 Heart rate Yes
62 ST segment Yes
63 Noninvasive BP Yes with accessories for adult , pediatric
& neon.

64 Invasive BP X2 Yes 2 with accessories

65 Temperature X2 Yes 2 with accessories
66 Pulse oximeter Yes with accessories
67 Capnography Yes numeric & graphic
68 Muscle relaxant Monitor NMT Yes
69 Number of channel Eight
70 Type Yes
71 Integrated Yes
72 Interface w/others Yes
73 DATA INPUT Rotary / Turn knob/Touch screen
74 Auxiliary outlets Yes, 2 - 4 OUTLETS
75 Back-Up Battery Yes
76 Type & Time Specify
77 ACCESSORIES Yes
78 Patient Circuit System Yes, Patient circuit for adult 3 sets,
pediatric circuit 3 sets & neonatal circuit
3 sets.

79 Anesthesia mask Yes, 3 sets for each size Adult, Pediatric

& Neonatal.

80 OTHER SPECIFICATION Complete set all size pressure cuff FDA,

CE, ISO Approved. All access needed.
81 Entropy , BIS or equivalent INCLUDED
82 C.O ITEMIZED WITH PATIENT MONITOR INCLUDED
1 ** GENERAL TERMS **
1.1 Unit must be FDA, CE marked.
1.2 If unit will be used invasively into patient: FDA must
be provided.

1.3 Medical Device must pass Clinical Trial in 3

Reference Hospitals for 3 months.

1.4 will not accept new devices not yet approved

Technically & Clinically as above.

1.5 Unit must be provided from an Exclusive agent or an

Authorized Representative.

1.6 Suppliers must Provide MDMA , MDNR Certificates

of the device from SFDA.

1.7 Suppliers must provide Evidence Proofs supporting

his capability offering Best Service.

1.8 Offers will not be accepted from a weak Suppliers not

having enough support team.