Eu Mdd Eu Md Class 1 On The Market 🇹🇷 Türkiye

Transparent I.V. Cathater Dressing (PU

Devices (same UDI-DI)
1
Certificates
1
Countries
32
Notified Bodies
1

Basic Information

Primary DI
08684032587221
Basic UDI-DI Code
B-08684032587221
Reference
20911
Device Types
Single use Sterile
Regulation
Eu Mdd
Classification
Eu Md Class 1
Status
On The Market

Additional Description

It is a sterile medical plaster used to fix the cannula and the catheter well in the vein and to ensure that the entry site is free from infection and trauma. Its hypoallergenic adhesive does not irritate the skin. It has a deep notch feature to fix the cannula and the blades of the catheter. Thanks to its transparent structure, it allows the catheter area to be controlled without changing the dressing. It easily adapts to the body contours and extends the usage time by moving with the body. It can be written on the cannula and the catheter to record the day they were first applied or the day they were changed. The products do not include any accessories. There are 2 sizes available on the Alban IV cannula dressing. (6cmx7cm, 7cmx8, 8cm According to 93/42/EEC directive Annex-IX Rule IV Classification Rule; They are all non-invasive devices that come into contact with injured skin and fall into Class I as they are used as a mechanical barrier for absorption or suppression of secretions. Classification on the basis of time; temporary - appliances intended for continuous use, normally less than 60 minutes.

CND Nomenclature Codes

Code Description
M04010202 POLYURETHANE FIXING DRESSINGS

Certificates

Type Number
MDD Annex V 2195-MED-1224502

Available In Countries

🇦🇹 Austria 🇧🇪 Belgium 🇧🇬 Bulgaria 🇨🇾 Cyprus 🇨🇿 Czechia 🇩🇪 Germany 🇩🇰 Denmark 🇪🇪 Estonia 🇬🇷 Greece 🇪🇸 Spain 🇫🇮 Finland 🇫🇷 France 🇭🇷 Croatia 🇭🇺 Hungary 🇮🇪 Ireland 🇮🇸 Iceland 🇮🇹 Italy 🇱🇮 Liechtenstein 🇱🇹 Lithuania 🇱🇺 Luxembourg 🇱🇻 Latvia 🇲🇹 Malta 🇳🇱 Netherlands 🇳🇴 Norway 🇵🇱 Poland 🇵🇹 Portugal 🇷🇴 Romania 🇸🇪 Sweden 🇸🇮 Slovenia 🇸🇰 Slovakia 🇹🇷 Türkiye 🇬🇧 United Kingdom

Similar Devices

Other on-the-market devices with the same classification (Eu Md Class 1) and regulation (EU MDD).

View all