User's Manual

EMC Guidance
The ME EQUIPMENT or ME SYSTEM is suitable for home healthcare environments.
Warning: Don’t be near the active HF surgical equipment and the RF shielded room of an
ME system for magnetic resonance imaging, where the intensity of EM disturbances is high.
Warning: Use of this equipment adjacent to or stacked with other equipment should be
avoided because it could result in improper operation. If such use is necessary, this
equipment and the other equipment should be observed to verify that they are operating
normally.
Warning: Use of accessories, transducers and cables other than those specified or provided
by the manufacturer of this equipment could result in increased electromagnetic emissions
or decreased electromagnetic immunity of this equipment and result in improper operation.
Warning: Portable RF communications equipment (including peripherals such as antenna
cables and external antennas) should be used no closer than 30 cm (12 inches) to any par
t
of the equipment TMB-2080 including cables specified by the manufacturer. Otherwise,
degradation of the performance of this equipment could result.
Technical description：
1. All necessary instructions for maintaining BASIC SAFETY and ESSENTIAL PERFOR-
MANCE with regard to electromagnetic disturbances for the excepted service life.
2. Guidance and manufacturer’s declaration-electromagnetic emissions and Immunity.
Table 1
Guidance and manufacturer’s declaration - electromagnetic emissions
RF emissions
CISPR 11
RF emissions
CISPR 11
Group 1
Class [ B ]
Class A
Comply
Compliance
Harmonic emissions
IEC 61000-3-2
Voltage fluctuations /
flicker emissions
IEC 61000-3-3
Emissions test
Authorised Component
please use the authorised adapter (Not included).
Input: 100-240V, 50-60Hz, 0.2A max
5V 1000 mA
Adapter
Type: BLJ06L050100U-B
Output:
For more information about our products,
please visit www.kinetikwellbeing.com
Contact Information
EU Declaration of Conformity (DoC)
Manufactured by:
Company:
Address:
Guangdong Transtek Medical Electronics Co., Ltd.
Zone A, No.105, Dongli Road, Torch Development District,
528437 Zhongshan, Guangdong, China
Guangdong Transtek Medical Electronics Co., Ltd.
Hereby, Transtek, declares that this blood pressure monitor is in
compliance with the essential requirements and other relevant
provisions of Radio Equipment Directive 2014/53/EU.
The declaration of conformity may be consulted at
https://usimg.bjyyb.net/sites/54000/54167/20210720090946176.jpg
AC adaptor
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EMC GUIDANCEAUTHORISED COMPONENT