Sterile adhesive wound dressing Non Wooven Biodress 5x7cm
Sterile non woven adhesive dressing with central non woven fabric coat.
Characteristics e properties:
Transpiring light and thin
X Ray transparent, permeable to air and vapour
hypoallergenic poly-acrylate adhesive central pad:
- non-woven folded fabric: has a higher power of absorption than cotton and does not fray at the edges
- fitted out with a polyester perforated anti-stick film: guarantees maximum absorption of blood or exudates and minimal possibility of adhesion to the wound.
Intended Use:
Sterile non-invasive type of devices, for short-term use, intended to be used as the control of microenvironment of a wound. Allow you to seal the wound along its entire perimeter and are indicated for application after surgery or traumatic injury.
Measure Code Packaging
cm 5x7 DRE12SBSR 100pcs/box, 1200pcs/carton
cm 8x10 DRE14SBSS 50pcs/box, 600pcs/carton
cm 8x15 DRE36SBSS 50pcs/box, 600pcs/carton
cm 10x15 DRE15SBSS 50pcs/box, 600pcs/carton
cm 10x20 DRE16SBSU 25pcs/box, 450pcs/carton
cm 10x25 DRE25SBSU 25pcs/box, 450pcs/carton
cm 10x30 DRE26SBSU 25pcs/box, 300pcs/carton
cm 10x35 DRE27SBSU 25pcs/box, 300pcs/carton
Technical data:
Composition of support Non woven dressing: 70% viscose + 30% polyester
Weight of support 50 g/m2 (typical value)
Minimum tensile strength 20 N/cm
The weight of the anti-tight fit of the retina of the central pad 15 g/m2 (typical value)
Composition of the central pad Non woven dressing 100% viscose
The total weight of the absorbent central pad (including the retina anti-tight fit)
Till to cm9x10cm: 110g/m2
Other than cm 9x10cm: 250 g/m2 (typical values)
Capacity of maximum absorption for the surface of the central absorbing pad 11 g/100 cm2 (typical value)
The weight of the hypo allergic adhesive i 23 g/mq ±5% (typical value)
Creep resistance <2.5 mm
Extensibility (N/cm) 10-12 N/cm (typical value)
Recommendations for use:
Before applying you should wash your hands thoroughly. Open the package and remove the protective paper. During the application of the dressing avoid touching the central pad. Center the absorbent fabric pad on the wound, adjust the adhesive to the clean and dry skin . Renew the dressing if necessary. Before the use, verify the integrity of the protective wrapping. In case of re-use it is possible to get an infection and you should consult a doctor.
Production standards:
Official Pharmacopoeia in force; Legislative Decree 46/97 on the application of Directive 93/42/EEC, Annex VII paragraph 3 and Annex V.
Sterilization: Ethylene oxide
Classification:
Legislative Decree 46/97 Medical Device classification for the purposes of EC marking the product in Class IIa.
Packaging:
- Primary Packaging: individually packed in a medical paper and box
- Secondary Packaging: carton
Storage:
Store in a clean, dry environment with a temperature not exceeding 50 ° C.
The hygienic conditions are ensured only in sealed confection.
Expiry date: 5 years from date of manufacture.
Waste Disposal:
Disposal must be carried out in accordance with national regulations.
Incineration or landfill should be carried out in controlled conditions. If the product is not in contact with infectious agents or other hazardous materials produces no toxic residue.
Manufacturer: Rays S.p.a
