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欲購買產品

medical equipments, mechanical equipments

欲購買產品之描述

A-Pulse Oximeter - 08 Nos

description:-

This is a portable patient monitor for monitoring oxygen saturation in the blood and pulse rate.
It shall monitor the oxygen saturation of arterial hemoglobin noninvasively by measuring the light absorbance changes resulting from arterial blood flow pulsations and display the oxygen saturation and pulse rate
The pulse oximeter shall display measurements of arterial spO2 from 0 to 100% and pulse rate in the range of 35 to 250bpm
The display of measurements of arterial spO2 at values from 80% to 100% shall be within an accuracy of 2% spO2, compared with fractional or functional oxygen saturation of an in vitro oximeter.
Pulse-rate measurements shall be in the range of 35 to 250 bpm with accuracy within ±1% or ±2 beats per minute (bpm)
If the monitor is unable to obtain an accurate reading, it shall clearly indicate this and, preferably, indicate the reason for the problem.
Pulse oximeter performance shall not be adversely affected by radiated or conducted electromagnetic interference (EMI) from nearby devices, especially high-frequency currents. At a minimum, the unit shall indicate that it is being affected by interference and shall not be damaged by the interference or affected after the interference ceases.
Pulse oximeter probes shall provide accurate spO2 and pulse-rate measurement in the presence of probe movement caused by the patient or by clinicians caring for the patient, or they should recognize and indicate motion artefact.
The spO2 and pulse-rate measurement accuracy shall not be affected by ambient thermal radiation or photoradiation (e.g., from surgical lights, radiant warmers, or bilirubin lights).
Measurements shall not be affected by light sources with modulation that may simulate physiologic signals.
The display shall be visible in bright or dim light, and the alarms shall be audible over background noise.
Pulse oximeters shall have audible alarms for high and low spO2, high and low pulse rate, and probe failure/disconnection that meet the following criteria.
The alarm sound level shall be at least 45 dB at a distance of 1 m.
The high spO2 alarm limit shall be adjustable from at least 90% to 100% spO2 .
The low spO2 alarm limit shall have a default setting no lower than 80% and shall be adjustable up to 95%, but no lower than 50%.
The high and low pulse rate alarm limit range shall be adjustable from 35 to 200 bpm.
It shall not be possible for the low spO2 or pulse-rate limit to be adjusted above the high spO2 or pulse rate limits.
The alarms shall sound when the measured spO2 or pulse rate is equal to the alarm-limit value or one digit above or below the alarm-limit value.
The alarm limits shall be displayed continuously, and each alarm condition will have a corresponding indication (e.g., display an explanatory message) to distinguish one condition from another.
All alarms should be fully explained in the operator's manual.
The user shall not be able to indefinitely disable or silence audible alarms.
The unit will clearly indicate any temporarily disabled alarm.
The pulse oximeters will sound a tone for each detected pulse, meeting the following criteria.
It should be easy to distinguish the pulse tone of the oximeter from the alarms.
It should be possible to adjust the volume of this tone or to silence it to prevent confusion with the QRS tone from a ECG monitor.
Ideally, the pitch of the pulse tone shall change with changing spO2.
The pulse oximeters shall indicate when spO2 and pulse-rate readings are likely to be inaccurate.
Special features or modes and alarm settings should be easy to operate and understand.
Battery back-up for the pulse oximeter should meet the following criteria.
The battery should operate the pulse oximeter for at least eight hours.
The battery will be recharged when the detector is operated by AC power.
A low-battery alarm should visibly indicate when the battery voltage falls to a level below which the unit may fail to perform satisfactorily.
The battery should not require more than 3 hours of recharging after depletion.
There should be a clear indication of the need for recharging; a readily visible indicator on the unit or charger should be provided to ensure that the batteries are being charged, not simply that the charger is plugged into an AC outlet.
The pulse oximeter will have a provision to protect against overcharging of the battery.
A battery-powered pulse oximeter should have a commonly available battery type that does not have to be replaced frequently.
The battery should be easy to recharge and/or replace.
Switching to battery power shall be automatic if line power fails.
The pulse oximeter shall function properly on line power after its battery is full depleted, shorted, or removed.
Pulse oximeters shall have a front-panel indicator to confirm that the unit is operating under battery or line power.
All information regarding battery replacement, preventive maintenance, and proper function should be included in the operator's and/or service manual.
Must be supplied with battery charging unit
Must be supplied with
Two each of compatible reusable finger probe with cable for adult and child
Both adult and paediatric cuff with tubes
2 spare batteries
Spare-parts and replacement parts for 2 years where necessary
Operational training
Technical training for maintenance staff

B- Autoclave,table top-10 Nos

Description:-

This is a tabletop steam sterilizer capable of sterilizing surgical instruments, hollow ware and linen materials
Instaclave Bench Top Model 2545 or substantially equivalent to the specification below
The sterilizer shall be electrically heated and controlled by a pressure switch but the programmes shall be microprocessor controlled
The sterilizer shall be fitted with a single door and mounted on a trolley.
The sterilizer shall perform air removal by displacement or gravity method, steam generation, sterilization, drying cycles and also flash sterilization.
The sterilizer should depend on only the inbuilt water reservoir for and steam generator for steam generation
The minimum selectable and controllable temperature range for sterilization shall be 121C to 135C(selectable sterilization temperature of 121oC with drying cycle and 134oC). this should automatically linked with the corresponding pressure.
Temperature, exposure time and venting shall be operator selectable, as a minimum parameters for standard sterilization; "flash" sterilization and drying cycles.
The following parameters should be displayed display: temperature, pressure and also include a cycle counter.
The following mechanism shall be included to ensure safety
Pressure relief valve
Overheat shutoff
Automatic cycle shut off
Low water shut off
The sterilizer shall meet or exceed all applicable ASME codes for pressure vessels.
The chamber shall be made of corrosion resistant material, and have minimum capacity of 22L.
Power consumption not exceeding 2.2kW
The sterilizer shall have at least three (3) internal corrosion resistant extendable shelves.
The sterilizer cabinet's external construction shall be stainless steel.
The tabletop steam sterilizer should come with all necessary installation hardware.
The supplier must include
mounting trolley with castors for installation
spare-parts for at least two years maintenance
portable air cooling water distillation unit
operational training
technical training for maintenance staff

公司介紹

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公司基本資料

公司名稱:	**********
聯絡人:	S.K.Bhatnagar
Email:	加入推薦信籃
電話:	**********
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國家:	India