Fylladerm Med Ster N / adher10x10
17.10€
20.12€
- Brand: SVAS BIOSANA SpA
- Product Code: 935210878
- EAN: 8004007001208
- Availability: In 10 - 14 Days
- Purchase 3 items for 16.76€ each
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FYLLA derm
NON-ADHERENT DRESSING
WITH NATURAL EXTRACTS
Description Fylladerm is a sterile, non-adherent dressing consisting of an open weave hydrophilic cotton gauze uniformly impregnated with a polyethylene glycol based ointment containing natural extracts.
Fylladerm determines an acceleration of tissue regenerative processes, as, thanks to its particular composition, it favors the migration of the cells preceding the formation of new tissue. The basic principle is to create a barrier effect, which allows the restoration of the optimal conditions for the cicatrization process.
Fylladerm does not adhere to the skin lesion and allows free drainage of the skin, allowing the passage of exudate to an absorbent secondary dressing. The dressing is well tolerated by the skin, conformable, adaptable and easily applicable.
Characteristics
Composition:
- Support: Hydrophilic cotton gauze with open weave. The warp (96 by 10 cm) and weft (94 by 10 cm) threads are suitably intertwined to minimize lint, in the event that the dressing is cut into the desired shape.
- Carrier: Ointment based on polyethylene glycols.
- Antioxidant: Tocopherol Acetate.
- Natural extracts: Dry extract of Centella Asiatica and Urtica Dioica.
Class of belonging of the Medical Device:
Class IIb ; as defined by rule 4 of Annex IX relating to Legislative Decree no. 46 of 24/02/1997 concerning Medical Devices. and subsequent amendments (Classification criteria, chapter III), point 1.4 (non-invasive devices in contact with the injured skin).
Clinical information
Indications for use
Fylladerm is particularly indicated in the topical treatment of dermal-epidermal tissue alterations that require the reactivation of epithelial neoformation processes, such as: skin wounds, pressure sores, ulcers and burns.
Contraindications
No local or systemic adverse reactions were observed during the clinical study.
Do not use in case of known sensitivity to the components of the product.
Replacement frequency
The frequency of dressing changes depends on the clinical condition of the cutaneous lesions and varies according to the clinical protocol indicated by the physician.
Fylladerm can be left in place even if the absorbent secondary dressing is changed.
Instructions for Use
Before applying Fylladerm it is necessary to clean the affected area.
Remove the dressing from the package, then apply gently, in single layers, directly in contact with the wound surface.
If necessary, cover with an absorbent secondary dressing and secure with bandage or plaster.
Warnings and Precautions:
In case of sensitization phenomena it is advisable to immediately suspend the treatment.
Keep the device out of the reach of children.
After use, do not dispose of the product in the environment.
Do not use if the package is not intact.
Do not leave the dressing in place for longer periods of time than recommended by the clinical protocol.
Sterilization
Sterilized device with beta rays according to a validated cycle that does not alter the characteristics of the product in compliance with the UNI EN ISO 11137 standard. The asterility is valid for 5 years.
Packaging
Each dressing is packaged in a single peel-open pouch.
NON-ADHERENT DRESSING
WITH NATURAL EXTRACTS
Description Fylladerm is a sterile, non-adherent dressing consisting of an open weave hydrophilic cotton gauze uniformly impregnated with a polyethylene glycol based ointment containing natural extracts.
Fylladerm determines an acceleration of tissue regenerative processes, as, thanks to its particular composition, it favors the migration of the cells preceding the formation of new tissue. The basic principle is to create a barrier effect, which allows the restoration of the optimal conditions for the cicatrization process.
Fylladerm does not adhere to the skin lesion and allows free drainage of the skin, allowing the passage of exudate to an absorbent secondary dressing. The dressing is well tolerated by the skin, conformable, adaptable and easily applicable.
Characteristics
Composition:
- Support: Hydrophilic cotton gauze with open weave. The warp (96 by 10 cm) and weft (94 by 10 cm) threads are suitably intertwined to minimize lint, in the event that the dressing is cut into the desired shape.
- Carrier: Ointment based on polyethylene glycols.
- Antioxidant: Tocopherol Acetate.
- Natural extracts: Dry extract of Centella Asiatica and Urtica Dioica.
Class of belonging of the Medical Device:
Class IIb ; as defined by rule 4 of Annex IX relating to Legislative Decree no. 46 of 24/02/1997 concerning Medical Devices. and subsequent amendments (Classification criteria, chapter III), point 1.4 (non-invasive devices in contact with the injured skin).
Clinical information
Indications for use
Fylladerm is particularly indicated in the topical treatment of dermal-epidermal tissue alterations that require the reactivation of epithelial neoformation processes, such as: skin wounds, pressure sores, ulcers and burns.
Contraindications
No local or systemic adverse reactions were observed during the clinical study.
Do not use in case of known sensitivity to the components of the product.
Replacement frequency
The frequency of dressing changes depends on the clinical condition of the cutaneous lesions and varies according to the clinical protocol indicated by the physician.
Fylladerm can be left in place even if the absorbent secondary dressing is changed.
Instructions for Use
Before applying Fylladerm it is necessary to clean the affected area.
Remove the dressing from the package, then apply gently, in single layers, directly in contact with the wound surface.
If necessary, cover with an absorbent secondary dressing and secure with bandage or plaster.
Warnings and Precautions:
In case of sensitization phenomena it is advisable to immediately suspend the treatment.
Keep the device out of the reach of children.
After use, do not dispose of the product in the environment.
Do not use if the package is not intact.
Do not leave the dressing in place for longer periods of time than recommended by the clinical protocol.
Sterilization
Sterilized device with beta rays according to a validated cycle that does not alter the characteristics of the product in compliance with the UNI EN ISO 11137 standard. The asterility is valid for 5 years.
Packaging
Each dressing is packaged in a single peel-open pouch.
CODE | SIZE (cm) | DRESSINGS FOR PACKAGING |
5SVASM520003 | 10 x10 | 10 BAGS |