EU2

Organization name

Neuromod Devices Limited

SRN

IE-MF-000004261

Manufacturer status

Active

8 warnings recorded — scroll inside the panel to see all entries.

• CW999

  Caution! – Do not use the device if you are pregnant, unless directed by a doctor.
• CW999

  Caution! – Do not use the device if you suffer from epilepsy or any other condition that may result in loss of consciousness.
• CW999

  Caution! – Do not use the device if you suffer from any condition that causes impaired sensitivity of the tongue.
• CW999

  Caution! – Do not use the device if you have lesions, sores, or inflammation of the oral cavity, unless directed by a doctor.
• CW999

  Caution! – Do not use the device if you have a pacemaker, defibrillator or any other active implantable device, unless directed by a doctor.
• CW999

  Contact between the Tonguetip and dental retainers or metal fillings may cause temporary discomfort.
• CW999

  Some people may experience a mild allergic reaction to the materials in the device. Note: The electrodes of the Tonguetip contain nickel.
• CW999

  You may experience a mild numbing sensation or a discomfort on the tongue during treatment. If this occurs, reduce the tongue stimulation. If the symptoms persist, contact your prescribing healthcare professional.

Primary placement in Ireland; available across 5 countries total.

Trade name

not provided

UDI-DI code

05391540580073

Basic UDI-DI

539154058TP-101-EU2ZG

Reference / catalog number

EU2

Issuing entity

GS1

Risk category

Class IIa

Applicable legislation

MDR [Regulation (EU) 2017/745 on medical devices]

Status

On the market

Quantity

1

Additional product description

ACCESSORY FOR TINNITUS TREATMENT DEVICE

Additional information URL

https://www.lenire.com/product-support/european-user-manuals-and-guides/

Clinical sizes

No clinical sizes registered for this device.

• Z12149099VARIOUS ENT INSTRUMENTS - OTHER

• Batch number
• Expiration date
• Manufacturing date
• Serial number
• Software identification