A&D TM-2441 Instruction Manual page 3

Recorder for ambulatory blood pressure monitor
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Compliance
Compliance with European Directive
The device conforms to Medical Devices Directive 93/42/EEC.
This is shown by the CE mark of conformity accompanied by
the reference number of a designated authority.
The device conforms to RoHS Directive 2011/65/EU.
The device conforms to Radio Equipment Directive 2014/53/EU.
Hereby, A&D Company, Limited declares that the device is in
compliance with Radio Equipment Directive 2014/53/EU.
The full text of the EU declaration is available at the following internet
address: https://www.aandd.jp/products/manual/manual_medical.html
Compliance with FCC Rules
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 = Federal Communications Commission in the U.S.A.)
FCC CAUTION
Changes or modifications not expressly approved by the party
responsible for compliance could void the user's authority to
operate the equipment. This transmitter must not be co-located
or operated in conjunction with any other antenna or transmitter.
This equipment complies with FCC radiation exposure limits set
forth for an uncontrolled environment and meets the FCC radio
frequency (RF) Exposure Guidelines. This equipment has very
low levels of RF energy that it deemed to comply without testing
the specific absorption ratio (SAR).
TM-2441
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