Reference. 94269DIFAIVCHG857
Chlorhexidine impregnated dressing 8.5cm x 7cm. Box of 25 units.
Transparent dressing indicated for antiseptic treatment thanks to its content in Chlorhexidine Digluconate gel.
Description
Transparent dressing indicated for treating central line puncture points and peripheral insertion catheters thanks to 2% Chlorhexidine Digluconate gel.
Features
- Supplied in 25 units per dispenser.
- Sterile, individually wrapped in sealed medical paper.
- Non-woven adhesive notches in reinforced polypropylene without latex, without bisphenol A and without phthalates (DEHP).
- Composed of transparent gel made of ionic polymer, chlorhexidine and glycerin.
- The reinforced frame is non-woven in reinforced polypropylene.
- Sterilized with ethylene oxide.
- The film is a transparent and semi-permeable polyurethane sheet.
Technical specifications
- Transparent and semi-permeable polyurethane sheet.
- Highly absorbent gel layer.
- Reinforced edges of non-woven fabric made in polypropylene.
- Hypoallergenic adhesive.
- Contains two notches for securing the catheter.
- Rounded corners for better adaptation to anatomically difficult areas and that prevent the dressing from easily peeling off.
- Contains a strip of non-woven fabric reinforced with polyurethane that allows to note the date of application of the dressing.
- Adheres to the skin, so it can be applied without secondary dressing fixing tapes.
- Can be removed without pain, trauma or residues on the skin.
- In vitro studies show bacteriostatic and fungistatic effect up to 7 days.
- Single use.
- Transparent to X-rays.
- Sterile.
Indications for use
- In vitro tests have shown that Difa® IV exhibits a bacteriostatic and fungistatic effect.
- Ideal for use during catheter application for the prevention of intravascular catheter-associated infections.
- They help secure and preserve the integrity of the devices, minimize movement and prevent catheter displacement.
- They are designed for the fixation of cannulas and catheters.
- 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.
Certificates:
- Class III medical device in accordance with European Directive MDD 93/42/EC.
- CE marked.
Features
- Supplied in 25 units per dispenser.
- Sterile, individually wrapped in sealed medical paper.
- Non-woven adhesive notches in reinforced polypropylene without latex, without bisphenol A and without phthalates (DEHP).
- Composed of transparent gel made of ionic polymer, chlorhexidine and glycerin.
- The reinforced frame is non-woven in reinforced polypropylene.
- Sterilized with ethylene oxide.
- The film is a transparent and semi-permeable polyurethane sheet.
Technical specifications
- Transparent and semi-permeable polyurethane sheet.
- Highly absorbent gel layer.
- Reinforced edges of non-woven fabric made in polypropylene.
- Hypoallergenic adhesive.
- Contains two notches for securing the catheter.
- Rounded corners for better adaptation to anatomically difficult areas and that prevent the dressing from easily peeling off.
- Contains a strip of non-woven fabric reinforced with polyurethane that allows to note the date of application of the dressing.
- Adheres to the skin, so it can be applied without secondary dressing fixing tapes.
- Can be removed without pain, trauma or residues on the skin.
- In vitro studies show bacteriostatic and fungistatic effect up to 7 days.
- Single use.
- Transparent to X-rays.
- Sterile.
Indications for use
- In vitro tests have shown that Difa® IV exhibits a bacteriostatic and fungistatic effect.
- Ideal for use during catheter application for the prevention of intravascular catheter-associated infections.
- They help secure and preserve the integrity of the devices, minimize movement and prevent catheter displacement.
- They are designed for the fixation of cannulas and catheters.
- 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.
Certificates:
- Class III medical device in accordance with European Directive MDD 93/42/EC.
- CE marked.








