Eu Mdr
Eu Md Class 3
On The Market
🇮🇹 Italy
Idroflog
Devices (same UDI-DI)
2
Certificates
1
Countries
1
Notified Bodies
1
Basic Information
- Primary DI
- 08058481370060
- Basic UDI-DI Code
- 805848137IDROFLOGAM
- Reference
- 5010097
- Device Types
-
Single use Sterile
- Regulation
- Eu Mdr
- Classification
- Eu Md Class 3
- Status
- On The Market
- Manufacturer
- Alfa Intes Industria Terapeutica Splendore S.r.l.
Additional Description
15 vials of 0,5 ml
CND Nomenclature Codes
| Code | Description |
|---|---|
| Q02030206 | EYE LUBRICANT SOLUTIONS |
Certificates
| Type | Number | Notified Body | Status |
|---|---|---|---|
| MDR Technical Documentation | CVD 0028-24 | ISTITUTO SUPERIORE DI SANITA' |
Available In Countries
🇮🇹 Italy
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.
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
Prontoderm® balíček
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