Chapter 8: Wireless Compliance
Publication Information
The information in this manual only applies to the VivaQuant Model RX‐1 device. Due to ongoing product improvements,
specifications in this manual are subject to change without notice.
TM
VivaQuant
and Rhythm Express
their respective owners.
Contact Information
For General Information and Customer
Service
VivaQuant
4339 Nancy Pl.
St. Paul, MN 55126
www.vivaquant.com
1‐866‐ECG‐TRUE (1‐866‐324‐8783)
Email: support@vivaquant.com
Part number (this manual) ‐ LP‐002 Revision B1
Part number (RX‐1) – 51‐0019
VivaQuant shall not be liable for errors contained herein or for incidental or consequential damages in connection with the
furnishing, performance, or use of this material.
VivaQuant makes no warranty of any kind regarding this material, included, but not limited to, the implied warranties or
merchantability and fitness for particular purpose.
This device complies with the FDA Unique Device Identification (UDI) system. Information identifying this device is
provided in the label adhered to the back of the device and on the device packaging. Device ID/SN is set by the
manufacturer and is secured from accidental modification.
Global Medical Device Nomenclature (GMDN)
GMDN
41651
TM
are trademarks of VivaQuant. All other marks referenced in this guide are owned by
30
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