Reference. 94269DIFAIVCHG67
Dressing impregnated with Chlorhexidine 6cm x 7cm. Box of 25 units.
Transparent dressing impregnated with Chlorhexidine. Thanks to its composition, it acts as an antiseptic treatment.
Description
Transparent dressing that contains a gel impregnated with 2% Chlorhexidine Digluconate that acts as an antiseptic treatment for puncture points of central routes and central catheters of peripheral insertion.
Features
- Supplied at 25 units per dispenser.
- Sterile, individually wrapped in sealed medical paper.
- Composed of transparent gel made of ionic polymer, chlorhexidine and glycerol.
- The film is a transparent and semi-permeable polyurethane sheet.
- The reinforced non-woven frame in reinforced polypropylene.
- The adhesive notches, non-woven in reinforced polypropylene without latex, without bisphenol A and without phthalates (DEHP).
- Sterilized with ethylene oxide.
Technical specifications
- Highly absorbent gel layer.
- Transparent and semi-permeable polyurethane sheet.
- Reinforced edges of non-woven fabric made in polypropylene.
- Rounded corners for better adaptation to anatomically difficult areas and that prevent the dressing from easily coming 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 placement of the dressing.
- In vitro studies show bacteriostatic and fungistatic effect up to 7 days.
- Sticks to the skin, so it can be applied without secondary dressing fixing tapes.
- It can be removed without pain, trauma or residues on the skin.
- Hypoallergenic adhesive.
- Transparent to X-rays.
- Sterile.
- Single use.
Indications for 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 facilitates its use and handling with gloves.
- They help ensure 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 the European MDD 93/42/EC Directive.
- CE marked.
Features
- Supplied at 25 units per dispenser.
- Sterile, individually wrapped in sealed medical paper.
- Composed of transparent gel made of ionic polymer, chlorhexidine and glycerol.
- The film is a transparent and semi-permeable polyurethane sheet.
- The reinforced non-woven frame in reinforced polypropylene.
- The adhesive notches, non-woven in reinforced polypropylene without latex, without bisphenol A and without phthalates (DEHP).
- Sterilized with ethylene oxide.
Technical specifications
- Highly absorbent gel layer.
- Transparent and semi-permeable polyurethane sheet.
- Reinforced edges of non-woven fabric made in polypropylene.
- Rounded corners for better adaptation to anatomically difficult areas and that prevent the dressing from easily coming 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 placement of the dressing.
- In vitro studies show bacteriostatic and fungistatic effect up to 7 days.
- Sticks to the skin, so it can be applied without secondary dressing fixing tapes.
- It can be removed without pain, trauma or residues on the skin.
- Hypoallergenic adhesive.
- Transparent to X-rays.
- Sterile.
- Single use.
Indications for 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 facilitates its use and handling with gloves.
- They help ensure 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 the European MDD 93/42/EC Directive.
- CE marked.







