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
- Manufacturer
- Medical Devices Technology International Ltd
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
ðŸ‡ðŸ‡· Croatia
ðŸ‡ðŸ‡º 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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