N
netseal
Hello elsmar forum,
in my new company we are developing a new anesthesia ventilator.
This machine is able to mix anesthesia gases, O2, N2O and Xenon together and vent it into the lung of the patient. The intended use includes an anesthetist standing near the machine all the time.
We have got a 17 inch display for command input and information output i.e. Gas concentrations, pressures, flows and the like.
The acting part of the machine consists of embedded devices and ist split into modules like: ventilation, gas mixer, alarm output, measurement devices etc.. I am responsible here for Hard/Software Development and
the conformance of development process and documentation.
The Riskmanagement Process states that there are no injuries to the patient are possible. So they started here the development of the whole
software with a classification A (IEC 62304).
My experiences in this field are small. I have developed a low risk device Class 2b/Software Class A and did the certification process earlier. Because this company had only experiences in development of medical gasmixing valves and indeed started with the development a PEMS without getting experienced developers into the company, I have
my debts about all this.
It would be very fine if the one or another could post their opinion here.
Florian Hillen
in my new company we are developing a new anesthesia ventilator.
This machine is able to mix anesthesia gases, O2, N2O and Xenon together and vent it into the lung of the patient. The intended use includes an anesthetist standing near the machine all the time.
We have got a 17 inch display for command input and information output i.e. Gas concentrations, pressures, flows and the like.
The acting part of the machine consists of embedded devices and ist split into modules like: ventilation, gas mixer, alarm output, measurement devices etc.. I am responsible here for Hard/Software Development and
the conformance of development process and documentation.
The Riskmanagement Process states that there are no injuries to the patient are possible. So they started here the development of the whole
software with a classification A (IEC 62304).
My experiences in this field are small. I have developed a low risk device Class 2b/Software Class A and did the certification process earlier. Because this company had only experiences in development of medical gasmixing valves and indeed started with the development a PEMS without getting experienced developers into the company, I have
my debts about all this.
It would be very fine if the one or another could post their opinion here.
Florian Hillen