Reference. 94269DIFAIVCHG10155
Chlorhexidine impregnated dressing 10cm x 15.5cm. Box of 25 units.
Transparent dressing impregnated with 2% Chlorhexidine Digluconate. Thanks to its composition, it acts as an antiseptic treatment.
Personal advice
Description
Transparent dressing that contains gel impregnated with 2% Chlorhexidine Digluconate that acts as an antiseptic treatment for central line and peripheral insertion central catheter puncture points.
Features
- The reinforced non-woven polypropylene frame.
- Sterile, individually wrapped in sealed medical paper.
- The film is a transparent and semi-permeable polyurethane sheet.
- Supplied in 25 units per dispenser.
- Sterilized with ethylene oxide.
- The adhesive notches without woven in reinforced polypropylene without latex, without bisphenol A and without phthalates (DEHP).
- Made of transparent gel composed of ionic polymer, chlorhexidine and glycerol.
Technical specifications
- Can be removed without pain, trauma or residue on the skin.
- Highly absorbent gel layer.
- Transparent and semi-permeable polyurethane sheet.
- Single use.
- Rounded corners for better adaptation to anatomically difficult areas and prevent the dressing from easily peeling off.
- Contains two holding notches that allow securing the catheter.
- Contains a strip of non-woven fabric reinforced with polyurethane that allows to note the date of dressing placement.
- In vitro studies show bacteriostatic and fungistatic effect up to 7 days.
- Adheres to the skin, so it can be applied without fixing tapes of secondary dressings.
- Reinforced edges of non-woven fabric made in polypropylene.
- Hypoallergenic adhesive.
- Transparent to X-rays.
- Sterile.
Indications of use
- 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 easier to use and handle with gloves.
- They help secure and preserve the integrity of devices, minimize movement and prevent catheter displacement.
- 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.
Certificates:
- Class III medical device according to European Directive MDD 93/42/EC.
- CE marked.
- The reinforced non-woven polypropylene frame.
- Sterile, individually wrapped in sealed medical paper.
- The film is a transparent and semi-permeable polyurethane sheet.
- Supplied in 25 units per dispenser.
- Sterilized with ethylene oxide.
- The adhesive notches without woven in reinforced polypropylene without latex, without bisphenol A and without phthalates (DEHP).
- Made of transparent gel composed of ionic polymer, chlorhexidine and glycerol.
Technical specifications
- Can be removed without pain, trauma or residue on the skin.
- Highly absorbent gel layer.
- Transparent and semi-permeable polyurethane sheet.
- Single use.
- Rounded corners for better adaptation to anatomically difficult areas and prevent the dressing from easily peeling off.
- Contains two holding notches that allow securing the catheter.
- Contains a strip of non-woven fabric reinforced with polyurethane that allows to note the date of dressing placement.
- In vitro studies show bacteriostatic and fungistatic effect up to 7 days.
- Adheres to the skin, so it can be applied without fixing tapes of secondary dressings.
- Reinforced edges of non-woven fabric made in polypropylene.
- Hypoallergenic adhesive.
- Transparent to X-rays.
- Sterile.
Indications of use
- 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 easier to use and handle with gloves.
- They help secure and preserve the integrity of devices, minimize movement and prevent catheter displacement.
- 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.
Certificates:
- Class III medical device according to European Directive MDD 93/42/EC.
- CE marked.








