Devices (same UDI-DI)
5
Certificates
0
Countries
0
Notified Bodies
0
Basic Information
- Primary DI
- 05017950000122
- Basic UDI-DI Code
- 050179500LBF_SterileUV
- Reference
- 3820
- Device Types
-
Single use Sterile
- Regulation
- Eu Mdr
- Classification
- Eu Md Class 1
- Status
- On The Market
- Manufacturer
- CliniMed Limited
Additional Description
LBF® Range is indicated for the protection of intact and injured skin that is at risk or likely to be compromised by corrosive bodily fluids (including urine and faeces) or adhesives
CND Nomenclature Codes
| Code | Description |
|---|---|
| M04010203 | SILICONE DRESSINGS |
Related Devices
The Basic UDI-DI associated with this device has 5 devices in total. Below are some other devices sharing the same Basic UDI-DI.
LBF® Sterile Barrier Film Foam Applicator 2ml
Device
EU MDR
·
Eu Md Class 1
·CliniMed Limited·On the market
LBF® Sterile No Sting Barrier Film Spray 30ml
Device
EU MDR
·
Eu Md Class 1
·CliniMed Limited·On the market
LBF® Sterile No Sting Barrier Film Spray 50ml
Device
EU MDR
·
Eu Md Class 1
·CliniMed Limited·On the market
LBF® Sterile Barrier Film Foam Applicator 1ml
Device
EU MDR
·
Eu Md Class 1
·CliniMed Limited·On the market
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