Reference. 94269DIFAIVCHG1012
Chlorhexidine impregnated dressing 10cm x 12cm. Box of 25 units.
Transparent dressing impregnated with Chlorhexidine. Thanks to its composition, it acts as an antiseptic treatment.
Description
Transparent dressing that contains gel impregnated with 2% Chlorhexidine Digluconate that acts as an antiseptic treatment for central line and peripheral central catheter puncture points.
Features
- Sterilized with ethylene oxide.
- Sterile, individually wrapped in sealed medical paper.
- The film is a transparent and semipermeable polyurethane sheet.
- Supplied in 25 units per dispenser.
- Composed of transparent gel made of ionic polymer, chlorhexidine, and glycerol.
- The reinforced frame is non-woven polypropylene.
- The adhesive notches are non-woven reinforced polypropylene without latex, bisphenol A, and phthalates (DEHP).
Technical specifications
- Transparent and semipermeable polyurethane sheet.
- Highly absorbent gel layer.
- Single-use.
- Rounded corners for better adaptation to anatomically difficult areas and prevent the dressing from easily peeling off.
- Contains two notches that allow securing the catheter.
- Reinforced edges of non-woven fabric made of polypropylene.
- Contains a strip of non-woven fabric reinforced with polyurethane that allows noting the date of dressing placement.
- In vitro studies show a bacteriostatic and fungistatic effect for up to 7 days.
- Adheres to the skin, so it can be applied without fixing tapes for secondary dressings.
- Can be removed without pain, trauma, or skin residues.
- Hypoallergenic adhesive.
- X-ray transparent.
- Sterile.
Indications for use
- 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.
- They are designed for the fixation of cannulas and catheters.
- Ideal for use during catheter application for the prevention of intravascular catheter-associated infections.
- In vitro tests have shown that Difa® IV exhibits a bacteriostatic and fungistatic effect.
Certificates:
- Class III medical device according to European Directive MDD 93/42/EC.
- CE marked.
Features
- Sterilized with ethylene oxide.
- Sterile, individually wrapped in sealed medical paper.
- The film is a transparent and semipermeable polyurethane sheet.
- Supplied in 25 units per dispenser.
- Composed of transparent gel made of ionic polymer, chlorhexidine, and glycerol.
- The reinforced frame is non-woven polypropylene.
- The adhesive notches are non-woven reinforced polypropylene without latex, bisphenol A, and phthalates (DEHP).
Technical specifications
- Transparent and semipermeable polyurethane sheet.
- Highly absorbent gel layer.
- Single-use.
- Rounded corners for better adaptation to anatomically difficult areas and prevent the dressing from easily peeling off.
- Contains two notches that allow securing the catheter.
- Reinforced edges of non-woven fabric made of polypropylene.
- Contains a strip of non-woven fabric reinforced with polyurethane that allows noting the date of dressing placement.
- In vitro studies show a bacteriostatic and fungistatic effect for up to 7 days.
- Adheres to the skin, so it can be applied without fixing tapes for secondary dressings.
- Can be removed without pain, trauma, or skin residues.
- Hypoallergenic adhesive.
- X-ray transparent.
- Sterile.
Indications for use
- 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.
- They are designed for the fixation of cannulas and catheters.
- Ideal for use during catheter application for the prevention of intravascular catheter-associated infections.
- In vitro tests have shown that Difa® IV exhibits a bacteriostatic and fungistatic effect.
Certificates:
- Class III medical device according to European Directive MDD 93/42/EC.
- CE marked.







