Eu Mdr
Eu Md Class 3
On The Market
๐ฎ๐น Italy
Repol Angimesh 0 - 6X11
Devices (same UDI-DI)
1
Certificates
1
Countries
7
Notified Bodies
1
Basic Information
- Primary DI
- 08033109710008
- Basic UDI-DI Code
- 3310971FT01HERPPLU
- Reference
- A0-6X11
- Device Types
-
Single use Sterile
- Regulation
- Eu Mdr
- Classification
- Eu Md Class 3
- Status
- On The Market
- Manufacturer
- ANGIOLOGICA B.M. S.R.L.
CND Nomenclature Codes
| Code | Description |
|---|---|
| P900202 | POLYPROPYLENE SURGICAL MESHES |
Certificates
| Type | Number | Notified Body | Status |
|---|---|---|---|
| MDR Technical Documentation | 025-00-00-MDR | ITALCERT SRL |
Available In Countries
๐จ๐ฟ Czechia
๐ฉ๐ช Germany
๐ฌ๐ท Greece
๐ช๐ธ Spain
๐ซ๐ท France
๐ฎ๐น Italy
๐ท๐ด Romania
Similar Devices
Other on-the-market devices with the same classification (Eu Md Class 3) and regulation (EU MDR).
MYOCARDIAL BIOPSY KITS
Device
EU MDR
·
Eu Md Class 3
·Joline GmbH & Co. KG·On the market·3 countries
Prontodermยฎ balรญฤek
Device
EU MDR
·
Eu Md Class 3
·On the market
Lifecath XS CT PICC Maestro
Device
EU MDR
·
Eu Md Class 3
·On the market
Lifecath XS CT PICC Maestro
Device
EU MDR
·
Eu Md Class 3
·On the market
Lifecath XS CT PICC Maestro
Device
EU MDR
·
Eu Md Class 3
·On the market
Lifecath XS CT PICC Maestro
Device
EU MDR
·
Eu Md Class 3
·On the market