Desmond,

Not as simple as your questions to explain I am afraid.  Below is a very
brief outline and by no means should be looked upon as detailing all the
issues.  Hope it helps.

A 2.4GHz spread spectrum device must comply with:
a)   ACA "Radiocommunications Class Licence (Spread Spectrum Devices)"
requirements with respect to transmitter operation/use.  The Class Licence
specifies transmitter characteristics (freq of operation and eirp limits
etc); and
b)   ACA "Radiocommunications (Electromagnetic Radiation - Human Exposure)
Standard 2001" (otherwise known s the HES or Human Exposure Standard)
requirements with respect to radiation characteristics (SAR etc).

No DoC is required regarding the Class Licence however a DoC and associated
Compliance Folder etc is required with respect to the EMR regulations.

NOTE:  The "host" equipment would naturally need to comply with Australian
safety, EMC and telecommunications regulations if applicable.

So, very brief answers to your questions concerning EMR requirements for the
spread spectrum device:
1.  Australian importer or their "Agent" need to establish a product
"Compliance Folder" and sign a DoC;
2.  C-tick mark required in terms of EMR;
3.  If overseas manufacturer/supplier of product does not have a local
office in Australia or where that local office is not the direct importer of
their product then the easiest solution is for:-
a)  overseas manufacturer/supplier (company A) to enter into agreement with
Australian organisation (company B) offering "Agent" services to Australian
importers (companies C); and
b)  for any Australian importer of overseas manufacturer's/supplier's
product to sign an "Agent" agreement with company B.
4.  The advantage of the arrangement outlined in 3 above is that company B
(offering "Agent" services) already has applied to use the C-Tick mark and
has been issued with a unique ACA Supplier Code to be used in association
with the C-Tick mark so the product need only one compliance label for all
Australian importers (otherwise, if each Australian importer assumes
compliance responsibility for the product they import the overseas supplier
is faced with having to label product for each importer separately - i.e.
different ACA Supplier Code for each importer);
5.  No fees in terms of approval submission fees if that is what you mean;
6.  No approval submittals required so no lead times there.  Under the
approach outlined in 3 above, the lead times are dependent upon how
quickly:-
a)  the overseas manufacturer can provide company B with the necessary
product information required for the Compliance Folder and satisfy them that
their product complies with all requirements; and
b)  "Agent" agreements are signed between at least one Australian importer
of the product (a company C described in point 3 above) and the "Agent"
(company B).

IMPORTANT NOTE:
Please do not use my CompuServe email address after 19 Apr 2002.
Effective immediately, my new email address is:   kevin.richard...@ieee.org

Sorry for any inconvenience and
Best regards,
Kevin Richardson

Stanimore Pty Limited
Compliance Advice & Solutions for Technology (including Australian Agent
Services)
(Legislation/Regulations/Standards)
Ph:       02-4329-4070       (Int'l: +61-2-4329-4070)
Fax:      02-4328-5639       (Int'l: +61-2-4328-5639)
Mobile:  04-1224-1620       (Int'l: +61-4-1224-1620)
Email:    kevin.richard...@ieee.org

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-----Original Message-----
From: owner-emc-p...@majordomo.ieee.org
[mailto:owner-emc-p...@majordomo.ieee.org]On Behalf Of Desmond Fraser
Sent: Thursday, 25 April 2002 10:27 AM
To: emc-p...@ieee.org
Subject: DSSS WLAN for Australia


Hello Group:



We recently received a certification granted for a 2.4 GHZ portable wireless
LAN card.  The device transmits between 2.4GHz and 2.472 GHz with maximum
EIRP levels of less than 15mW.  This device was FCC approved under 15.247,
Specific absorption rate measurements were also performed.



Does anyone know the following below for Australia.



1.                   Can the manufacturer use a DOC with an Australian
agent?



2.                   Is the ctick-mark mandatory for the referenced devices?



3.                   Should an agency agreement exist between agent and the
manufacturer?



4.                   Who applies for the Ctick mark?  The agent or the
manufacturer.



5.                   Are there any fees involved?



6.                   What is the typical time frames from submitting to
actual approval.



Thanks in advance



Desmond A. Fraser

Rhein Tech Labs, Inc.

360 Herndon PKWY, Suite 1400

Herndon, VA 22070

Tel: 703-689-0368

Fax: 703-689-2056

mailto:desm...@rheintech.com



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