I
How to use this manual
This user’s manual explains the functions of the InBody R20
Ⓑ
.
Follow the instructions below for effective use this manual.
1. Please read all the instructions in this manual thoroughly before operation.
2. Fully utilize the helpful materials, such as the diagrams and illustrations, to get a clear
understanding of the product.
3. Before calling Biospace for assistance,
please refer to “ Chapter 11. One-minute check before calling for service ”.
4. If you have clinical issues while using the InBody R20Ⓑ, please contact us using the e-mail
address as shown below.
E-mail : usa@biospaceamerica.com TEL: 323-932-6503
5. Most importantly, please read the instructions and become familiar with the following notations:
Information
1. This product has been designed, manufactured, and inspected under the full quality assurance
system of Biospace. Biospace fulfills European MDD(Medical Device Directive), and InBody R20Ⓑ
has acquired the CE conformity marking.
2. This equipment may cause the above mentioned medical devices to malfunction.
3. This equipment may cause harmful interference to other devices in the vicinity if not installed and
used in accordance with the installation specifications. However, there is no guarantee that the
interference will not occur for a particular installation.
4. The InBody R20Ⓑ has been designed, manufactured, and inspected under the full quality
assurance system of Biospace. Biospace fulfills the international standardization system, ISO 90001
and ISO 13485.
5. The InBody R20Ⓑ fulfills the Standards of IEC60601-1(EN60601-1), Safety of Electric Medical
Equipment. In addition, the InBody R20Ⓑ complies not only with Level A for Noise Immunity, but also
with Level A for Noise Emission by the Standard IEC60601-1-2(EN60601-1-2), Electromagnetic
Compatibility Requirements.