Tech Specs

Looking for all the details you can handle? You’ll find them right here in our tech specs.

Output

Waveform

Biphasic with alternating leading phase, symmetrical, rectangular

Regulated Current or Voltage

Current

Net Charge per Pulse

0 ± 1 μC into 500Ω Load

Maximum Output Voltage (±10%)

100V

Maximum Output Current (<1KΩ load) (±10%)

100 mA

Pulse Duration (±4%)

200 - 400 μsec

Pulse Frequency (±4%)

60-100 Hz, randomly varying

Pulse Pattern

Continuous

Maximum Phase Charge

20 μC

Maximum Current Density

0.71 mA/cm² into 500Ω load

Maximum Average Current

4 mA into 500Ω load

Maximum Average Power Density

7 mW/cm² into 500Ω load

Output Trips

No Load

Device not connected to patient

Insufficient Charge

Delivered charge below target

Over Load

Delivered charge above target

Electrode Peeling

Electrode dislodging from skin

Therapy Session

Timer

60 minutes

Start Therapy

Click button once

Stop Therapy

Click button 4 times

Manual Intensity Increase/Decrease

Increase +1.25% per second, decrease -5%

Habituation Compensation

Adaptive stepwise increase in intensity during session

Electrode

Type

Self-adhering, single-patient use, multiple applications

Materials

Maylar substrate, silver electrode pads

Number of Electrodes

2, outer electrode area 28 cm², inner electrode area 33 cm²

Connector

Medical snap (male)

Dimensions

0.2 cm x 5.3 cm x 28.3 cm (exterior)

Power

Source

Permanent rechargeable battery

Battery Type

Rechargeable 3.7V Lithium-Ion battery

Battery Life

400 Charge Cycles

Charging Source

AC line adapter

Line Current Isolation

Patient disconnected when charging

Patient Leakage Current, DC

<10 μA

Patient Leakage Current, Enclosure

<10 μA

Physical

Dimensions

98 mm x 74 mm x 11 mm

Weight (without straps)

62g

Environmental

IP Classification

IP20

Operating Temperature Range

-5° C to 40° C

Atmospheric Pressure Range

70 kPa to 106 kPa

Relative Humidity Range

15% to 93%

Transport and Storage Temperature Range

-25° C to 70° C

Atmospheric Pressure Range

70 kPa to 106 kPa

Relative Humidity Range

10% to 93%

Guidance Documents & Standards

FDA

Draft Guidance for Industry and Staff: Class II Special Control Guidance Document: Transcutaneous Electrical Nerve Stimulator for Pain Relief (April 5, 2010)

IEC

IEC 60601-1, IEC 60601-1-2, IEC 60601-1-6, IEC 60601-1-11, IEC 62304

Bluetooth®

The Bluetooth word mark and logos are owned by the Bluetooth SIG, Inc. and any use of such marks by NeuroMetrix, Inc. is under license.

Communication between the Quell device and the Smartphone is via Bluetooth.

 

Disabling Bluetooth

While all sensitive data transmission is encrypted, Bluetooth functionality can be turned off for increased privacy. If Bluetooth is disabled, then the Quell Relief App will not function, but all other functions of the Quell device will operate normally.

 

To turn off Bluetooth:

  1. Plug the Quell device into the charger/wall outlet,
  2. Click and hold the button on the Quell device for approximately 10 seconds until the one orange and one white LED light up, then release the button.
  3. The Bluetooth module is now disabled.

To reactivate Bluetooth functionality, repeat the above steps. All six LED’s should be lit.

Bluetooth Specifications

Bluetooth Module

Bluegiga BLE 113 Bluetooth® Module with Bluetooth® 4.0 low energy radio

Transmit Power

+0 dBm

Receiver Sensitivity

-93 dBm

FCC Rules

Part 15C

Frequency Range

2402.0 - 2480.0

Output Watts

0.0011

Security

Encryption

Quell App requires iOS version 8.0 or later or Android version 4.4 or later
Smartphone must support Bluetooth LE

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He Simply Lost Hope Until Quell

For two years, my husband was in severe pain due to nerve damage from shingles. His pain was excruciating … Within one hour of starting Quell, his pain went from an 8 to a very mild 1. He is happy and slowly returning to the person his family loves!

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