Eu Mdr Eu Md Class 1 On The Market

Femmeze

Devices (same UDI-DI)
2
Certificates
0
Countries
32
Notified Bodies
0

Basic Information

Primary DI
15060228630191
Basic UDI-DI Code
50602240075GL
Reference
40075
Device Types
Sterilization
Regulation
Eu Mdr
Classification
Eu Md Class 1
Status
On The Market

Additional Description

Single patient use device for self-management of pelvic organ prolapse (Rectocele). A rectocele occurs when the rectum wall bulges into the vagina (pelvic organ prolapse) in women. The device is used to replace the use of fingers. Manual vaginal rectocele reduction instrument that is reusable and removable that is placed into vagina temporarily to train back or re-align the rectum tissue to treat a rectocel.

CND Nomenclature Codes

Code Description
U070399 PELVIC FLOOR REHABILITATION DEVICES - OTHER

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 2 devices in total. Below are some other devices sharing the same Basic UDI-DI.

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