Eu Mdr Eu Md Class 1 On The Market

Femmax Biege

Devices (same UDI-DI)
3
Certificates
0
Countries
32
Notified Bodies
0

Basic Information

Primary DI
50602286300192
Basic UDI-DI Code
5060224006ZD
Reference
40064
Device Types
Sterilization
Regulation
Eu Mdr
Classification
Eu Md Class 1
Status
On The Market

Additional Description

Providing feminine care for women of all ages, BPA and Latex free. The Femmax vaginal dilators/trainers are for use as a manual, reusable device placed into the vagina temporarily to reduce the formation of adhesions after pelvic radiotherapy and to train the vaginal muscles through stretching the vaginal opening when using for psychosexual therapy. The device can also help with other conditions affecting the vulva/vagina.

CND Nomenclature Codes

Code Description
L0509020101 VAGINAL DILATORS, REUSABLE

Available In Countries

🇦🇹 Austria 🇧🇪 Belgium 🇧🇬 Bulgaria 🇨🇾 Cyprus 🇨🇿 Czechia 🇩🇪 Germany 🇩🇰 Denmark 🇪🇪 Estonia 🇬🇷 Greece 🇪🇸 Spain 🇫🇮 Finland 🇫🇷 France 🇭🇷 Croatia 🇭🇺 Hungary 🇮🇪 Ireland 🇮🇸 Iceland 🇮🇹 Italy 🇱🇮 Liechtenstein 🇱🇹 Lithuania 🇱🇺 Luxembourg 🇱🇻 Latvia 🇲🇹 Malta 🇳🇱 Netherlands 🇳🇴 Norway 🇵🇱 Poland 🇵🇹 Portugal 🇷🇴 Romania 🇸🇪 Sweden 🇸🇮 Slovenia 🇸🇰 Slovakia 🇹🇷 Türkiye 🇬🇧 United Kingdom

Related Devices

The Basic UDI-DI associated with this device has 3 devices in total. Below are some other devices sharing the same Basic UDI-DI.

Similar Devices

Other on-the-market devices with the same classification (Eu Md Class 1) and regulation (EU MDR).

View all