Eu Mdr Eu Md Class 2a On The Market

Alivia

Alivia is a medical device designed to be used in the home healthcare environment to treat symptoms of urinary and/or faecal incontinence and is suitable for use by all who can control the device and understand the instructions. Alivia may also help to relieve the pain of secondary menstrual pain due to conditions such as endometriosis, fibroids or pelvic inflammatory disease.

Devices (same UDI-DI)
1
Certificates
0
Countries
0
Notified Bodies
0

Basic Information

Primary DI
05033435135967
Basic UDI-DI Code
5033435K00138ZU
Reference
K-ALIVIA
Device Types
None provided
Regulation
Eu Mdr
Classification
Eu Md Class 2a
Status
On The Market

Additional Description

The Alivia is a powered muscle stimulator used for strengthening the pelvic floor muscles. It sends a gentle stimulation (similar to your natural nerve impulses) direct to your pelvic floor muscles through a vaginal probe with stainless steel electrodes. These signals make your pelvic floor muscles contract. If you have forgotten how to contract them, are having trouble getting muscle response, or simply want to bring back the condition of your pelvic floor muscles, the Alivia can work them for you to build up their strength and help you to develop your own muscle control. It perfectly complements pelvic floor exercises. The Alivia is very easy to use, with four clearly labelled preset training programmes, a fifth programme for period pain and a simple push button control.

Medical Purpose

Alivia is a medical device designed to be used in the home healthcare environment to treat symptoms of urinary and/or faecal incontinence and is suitable for use by all who can control the device and understand the instructions. Alivia may also help to relieve the pain of secondary menstrual pain due to conditions such as endometriosis, fibroids or pelvic inflammatory disease.

CND Nomenclature Codes

Code Description
U070399 PELVIC FLOOR REHABILITATION DEVICES - OTHER

Similar Devices

Other on-the-market devices with the same classification (Eu Md Class 2a) and regulation (EU MDR).

View all