Canon BM70659 用户手册

下载
页码 2
9. Regulatory information
38
9-2. Radio frequency (RF) compliance information
U.S.A.
FCC Part 15 Subpart B Class A and Part 15 Subpart C/E 
(RF Exposure).
Canada
RSS-210
European Union (and EEA)
ETSI EN300 328
ETSI EN301 489
ETSI EN301 893
Australia
AS4268
Singapore
IDA TS SRD
„ FCC compliance (For U.S.A.)
Contains FCC ID:AZDBM70659
This device complies with Part 15 of the FCC Rules. Operation is subject to the 
following two conditions: (1) this device may not cause harmful interference. And (2) 
this device must accept any interference received, including interference that may 
cause undesired operation.
FCC WARNING:
Changes or modifications not expressly approved by the party responsible for 
compliance could void the user’s authority to operate the equipment.
Note: This equipment has been tested and found to comply with the limits for a Class A 
digital device, pursuant to part 15 of the FCC Rules. These limits are designed to 
provide reasonable protection against harmful interference when the equipment is 
operated in a commercial environment. This equipment generates, uses, and can 
radiate radio frequency energy and, if not installed and used in accordance with the 
instruction manual, may cause harmful interference to radio communications. 
Operation of this equipment in a residential area is likely to cause harmful interference 
in which case the user will be required to correct the interference at his own expense.
5.15-5.25GHz band is restricted to indoor operations only.
This transmitter must not be co-located or operated in conjunction with any other 
antenna or transmitter.
RF exposure compliance
The available scientific evidence does not show that any health problems are 
associated with using low power wireless devices. There is no proof, however, that 
these low power wireless devices are absolutely safe. Low power wireless devices emit 
low levels radio frequency energy (RF) in the microwave range while being used. 
EN 60601-1-4:1996+A1:1999
Medical electrical equipment - Part 1-4:Collateral 
Standard:Programmable electrical medical systems
EN 60601-1-6:2007
Medical electrical equipment - Part 1-6:Collateral Standard:Usability
EN 60601-2-32:1994
Medical electrical equipment - Part 2: Particular requirements for the 
safety of associated equipment of X-ray equipment
EN 62304:2006
Medical device software-Software life cycle processes
EN 62366:2008
Medical device - Application of usability engineering to medical 
devices
EN ISO 14971:2009
Medical device - Application of risk management to medical devices
EN ISO 10993-1:2009/-5:2009/
10993-10:2009
Biological evaluation of medical devices Part 1: Evaluation and 
testing within a risk management process