FDA UDI In Commercial Distribution 🇺🇸 United States

Rhythm Express

DI: 00860000272414 · Model: RX-1 · VIVAQUANT, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Rhythm Express
Primary DI
00860000272414
Version / Model
RX-1
Company Name
VIVAQUANT, INC.
Labeler DUNS
832287945
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-03-18
Public Version
2
Public Version Date
2019-05-07
Public Version Status
Update
Public Device Record Key
84428ca3-8da4-4df5-b8cf-fe18c387b39d

Device Description

The Rhythm Express RX-1 will be worn by adult patients for a period of time as prescribed by a physician, typically 1 day to 4 weeks, and will continuously monitor ECG. RX-1 will function in one of three modes: a) Mobile Cardiac Telemetry (MCT), b) Event Recorder (ER), and Wireless Holter (WH). The device will connect to standard ECG electrodes to capture 2 channel ECGs. An embedded algorithm processes the acquired ECG to detect arrhythmias, compress the ECG, and remove most in-band noise without distorting ECG morphology. RX-1 incorporates a cellular modem to communicate with the RS-1 Web Service. The RX-1 device uses an embedded cellular modem on the Verizon LTE network. The RX-1 device is not a life-supporting or life-sustaining system. Clinical judgment and experience are used to check and interpret the data.

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
MR Unsafe
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
DXH Transmitters And Receivers, Electrocardiograph, Telephone

GMDN Terms

Code Name
36367 Electrocardiography telemetric monitoring system transmitter

Identifiers

Type ID
Primary 00860000272414

Premarket Submissions

Submission Number Supplement Number
K183704 000