Reference. 94269DIFAIVCHG85115A
Chlorhexidine impregnated dressing 8.5cm x 11.5cm. Box of 25 units.
Transparent dressing designed for antiseptic treatment impregnated with 2% Chlorhexidine Digluconate gel.
Description
Transparent dressing specially designed to treat central line puncture points and also indicated for peripheral insertion catheters.
Features
- Sterile, individually wrapped in sealed medical paper.
- Supplied in 25 units per dispenser.
- Sterilized with ethylene oxide.
- Non-woven adhesive notches in reinforced polypropylene without latex, without bisphenol A and without phthalates (DEHP).
- The reinforced non-woven frame in reinforced polypropylene.
- Composed of transparent gel made of ionic polymer, chlorhexidine and glycerol.
- The film is a transparent and semi-permeable polyurethane sheet.
Technical specifications
- Highly absorbent gel layer.
- Transparent and semi-permeable polyurethane sheet.
- Hypoallergenic adhesive.
- Single use.
- Reinforced edges of non-woven fabric made in polypropylene.
- Contains two holding notches that allow securing the catheter.
- Rounded corners for better adaptation to anatomically difficult areas and prevent the dressing from easily peeling off.
- Contains a strip of non-woven fabric reinforced with polyurethane that allows to note the date of dressing placement.
- Adheres to the skin, so it can be applied without secondary dressing fixation tapes.
- It can be removed without pain, trauma or residues on the skin.
- In vitro studies show bacteriostatic and fungistatic effect up to 7 days.
- X-ray transparent.
- Sterile.
Indications for use
- Ideal for use during catheter application for the prevention of intravascular catheter-associated infections.
- Designed for the fixation of cannulas and catheters.
- Help secure and preserve the integrity of devices, minimize movement and prevent catheter displacement.
- The application frame facilitates its application and prevents it from sticking to gloves or itself. This makes it easy to use and handle with gloves.
- In vitro tests have shown that Difa® IV exhibits a bacteriostatic and fungistatic effect.
Certificates:
- Class III medical device in accordance with European Directive MDD 93/42/EC.
- CE marked.
Features
- Sterile, individually wrapped in sealed medical paper.
- Supplied in 25 units per dispenser.
- Sterilized with ethylene oxide.
- Non-woven adhesive notches in reinforced polypropylene without latex, without bisphenol A and without phthalates (DEHP).
- The reinforced non-woven frame in reinforced polypropylene.
- Composed of transparent gel made of ionic polymer, chlorhexidine and glycerol.
- The film is a transparent and semi-permeable polyurethane sheet.
Technical specifications
- Highly absorbent gel layer.
- Transparent and semi-permeable polyurethane sheet.
- Hypoallergenic adhesive.
- Single use.
- Reinforced edges of non-woven fabric made in polypropylene.
- Contains two holding notches that allow securing the catheter.
- Rounded corners for better adaptation to anatomically difficult areas and prevent the dressing from easily peeling off.
- Contains a strip of non-woven fabric reinforced with polyurethane that allows to note the date of dressing placement.
- Adheres to the skin, so it can be applied without secondary dressing fixation tapes.
- It can be removed without pain, trauma or residues on the skin.
- In vitro studies show bacteriostatic and fungistatic effect up to 7 days.
- X-ray transparent.
- Sterile.
Indications for use
- Ideal for use during catheter application for the prevention of intravascular catheter-associated infections.
- Designed for the fixation of cannulas and catheters.
- Help secure and preserve the integrity of devices, minimize movement and prevent catheter displacement.
- The application frame facilitates its application and prevents it from sticking to gloves or itself. This makes it easy to use and handle with gloves.
- In vitro tests have shown that Difa® IV exhibits a bacteriostatic and fungistatic effect.
Certificates:
- Class III medical device in accordance with European Directive MDD 93/42/EC.
- CE marked.








