All

The DRAFT for the revised 3551 as released for public comment yesterday.

It can be found on the Standards Australia website at www.standards.org.au 
- the link to drafts for comment is on the left hand margin.

Accessing the draft requires creatino of a login, but that is only an 
email and a password, and downloads of the draft are FREE.

Look for DR 10023.

Over the next few weeks, the College of Biomedical Engineering will be 
running consultation workshops in each state to encourage comment while 
there is still time to make changes - watch for advice from State Division 
Rep's.  All are welcome.

Dates are 

Brisbane        28 June
Sydney          1 July
Melbourne       5 July
Adelaide        8 July
Perth           July 12 (tentative)

Regards

Michael Flood

Chairman, College of Biomedical Engineering
Engineers Australia




"Bruce Morrison" <[email protected]> 
17/06/2010 14:13
Please respond to
<[email protected]>


To
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Subject
[bmelist] AS3551 Testing versus Manufacturer Service Recommendations





Hi Owen

I would like to hope that we could have "profession endorsed" procedures 
for
all types of devices but fear that the profession will be extinct before 
it
happens. We have had several attempts, beginning with the recommended
parameters to test in the back of the original 1986 (was it '86?) AS-3551.
We have talked about risk management and had attempts to have dialogue 
with
ACHS and Work Cover in some states but still no agreement.

It seems to me that a measure of the success of the College of BME, the
SMBEs and the BEAGs around the country would be that we have achieved this 
-
but we haven't so therefore we haven't been successful in this area.

I think we need to divorce the risk management argument from the
test/inspect/PM argument and leave the decision on whether to test, 
inspect
or PM to individual health facilities, regions, states, etc. We should
define the parameters but only in a broad way - pretty much like we did in
the original AS-3551 but expanded to other types of equipment including
pneumatic equipment. So, for example, we would say that a manual
sphygmomanometer (aneroid) needs to have a physical inspection, and its
accuracy and leak rate checked - how you do it and with what test 
equipment
would be up to the individual service. How often could be subject to
suggestions based on such things as the frequency of use, the wear and 
tear
it receives from driving around in an ambulance (particularly on rough
country roads or in countries where the term road is more of a hope than a
reality), the criticality of the measurement, fluid or energy delivery, 
etc.

So if the aneroid sphygmomanometer sits in a dermatology OPD Clinic
consulting room and doesn't move too much and doesn't get used much and
maybe the results from taking of BPs on patients with skin problems is 
less
critical than in the Cardiology Clinic next door, then maybe don't check 
it
so often.

So what I'm saying is develop a professional guideline as to how to
determine these things and leave it to the individual to do it or not. 
Note
- I'm not saying risk management - basically because I don't like the 
term.
Also, none of this is new but I thought I would say it again!

As for the O2 and air flowmeters, we have them tested every year by an
outside provider and I think we find many more leaking than being
inaccurate, and in the case of the O2 flowmeters, I guess that saves us
money on the purchase of oxygen.

Cheers

Bruce.

Bruce Morrison
Medical Equipment Specialist
Ministerio da Saude
Timor-Leste
Phone: +670 753 2189



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