Devices (same UDI-DI)
1
Certificates
1
Countries
17
Notified Bodies
1
Basic Information
- Primary DI
- 07798121803558
- Basic UDI-DI Code
- B-07798121803558
- Reference
- KIT-UT-01
- Device Types
-
Single use Sterile
- Regulation
- Eu Mdd
- Classification
- Eu Md Class 3
- Status
- On The Market
- Manufacturer
- PROMEDON S.A.
Additional Description
Splentis is intended for transvaginal reestablishment and reinforcement of the physiologic anatomy of the female pelvic floor in the defined patient population.
CND Nomenclature Codes
| Code | Description |
|---|---|
| P900202 | POLYPROPYLENE SURGICAL MESHES |
Certificates
| Type | Number | Notified Body | Status |
|---|---|---|---|
| MDD Annex II (excluding section 4) | HD 60150769 0001 | TรV Rheinland LGA Products GmbH | Expired |
Available In Countries
๐ฆ๐น Austria
๐จ๐ฟ Czechia
๐ฉ๐ช Germany
๐ฉ๐ฐ Denmark
๐ช๐ช Estonia
๐ฌ๐ท Greece
๐ช๐ธ Spain
๐ซ๐ฎ Finland
๐ซ๐ท France
๐ฎ๐น Italy
๐ณ๐ฑ Netherlands
๐ณ๐ด Norway
๐ต๐น Portugal
๐ท๐ด Romania
๐ธ๐ช Sweden
๐ธ๐ฎ Slovenia
๐น๐ท Tรผrkiye
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