Prontosan® Wound Gel X

Lasting wound protection and hydration – even between dressing changes

Prontosan® Gel X is a highly viscous, sterile wound gel designed for the intensive care of acute and chronic wounds such as pressure ulcers, diabetic foot ulcers, surgical wounds, and burns.

Formulated with Polihexanide and Betaine, it offers long-lasting cleansing, moisturising and antimicrobial action even between dressing changes.

Helps eliminate and prevent biofilm, reduces odour and pain, and supports faster healing in stalled or complex wounds.

Key Benefits:

• Disrupts and prevents formation of biofilm
• Provides sustained antimicrobial barrier
• Helps reduce risk of infection and complications
• Reduces healing time, wound odour and pain
• Facilitates gentle dressing changes
• Compatible with commonly used wound dressings

Indications:

• Infected and non-infected acute or chronic wounds
• Diabetic, vascular, pressure ulcers
• Post-surgical wounds (with or without sutures)
• Burns – thermal and non-thermal (I, IIa, IIb, III)
• Fistulas, abscesses and cavity wounds

Available formats:

• 50g tube
• 250g tube

Directions for Use:

1. Wash your hands and, if possible, cleanse the wound using Prontosan® Irrigation Solution.
2. Apply an appropriate amount of Prontosan® Gel X directly to the wound or into cavities.
3. Cover with a sterile and appropriate wound dressing.
4. Reapply with each dressing change (once or twice daily or as instructed by your healthcare professional).

Do not mix with other topical products. For external use only.

Combined Use with Prontosan® Irrigation Solution:

For optimal results in biofilm management and wound bed preparation, use Prontosan® Irrigation Solution to irrigate the wound before applying Prontosan® Gel X.

This combination offers:

• Immediate wound cleansing and hydration
• Prolonged antimicrobial protection between dressing changes
• Improved control of pain, inflammation and odour

This approach follows internationally recognised protocols for wound bed preparation (WBP).

Trust & Certification:

• Certified under the EU MDR 2017/745 Regulation
• Class III Medical Device – suitable for serious and complex wounds
• Clinically evaluated and approved by a Notified Body
• Trusted in hospitals and home care settings
• Proven biofilm management supported by clinical studies

This product is not intended to replace medical advice. Always consult your healthcare provider before use.