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Biatain Silicone
Adhesive polyurethane foam.
Manufactured without natural rubber latex.
It does not contain phthalates.
Description
The new Biatain Silicone is a multi-layered absorbent dressing consisting of two absorbent layers, two layers in polyurethane film, one external and one internal, and a pressure-sensitive adhesive (PSA) that holds together the two absorbent layers.
The last layer, in contact with the injury and the skin, is made of delicate silicone perforated adhesive.
The first absorbent layer, covered in perforated silicone, consists of Biatain polyurethane foam, multilayered, hydrophilic, with vertical alveolar structure.
Thanks to the special 3D vertical alveolar technology it absorbs and avoids the release of the exudate even under compression, thus creating the ideal humid environment for the healing process of the injury, and avoiding the maceration of the perilesional skin.
Polyurethane foam is positioned without steps at the same level of injury avoiding any pressure marks on the perilesional skin.
In contact with the exudate the foam conforms optimally to the lesion bed reducing the dead spaces where bacteria can nest.
The second absorbent layer, superior to the first, in contact with the external polyurethane film, is a superabsorbent hydrocapillary buffer consisting of polyethylene, cellulose fibre (CMC) and SAP (Super Absorbent particles in sodium polyacrylate polymers).
The instantaneous absorption of the excess exudate that passes through the first layer of polyurethane foam, gives the effect of hydrocapillary to the super absorbent tampon: fluids are absorbed vertically and distributed both vertically and horizontally.
In fact, cellulose and SAP polymers in contact with the exudate change phase, freezing.
The gel that is formed allows to maintain the optimal humid environment for the healing of injuries and to ensure a high level of retention even under compression.
The two absorbent layers are held together by the PSA, Sensitive Pressure Sticker, which prevents the delamination of absorbent layers when they come into contact with moisture following the absorption of the exudate.
The external polyurethane film layer, in direct contact with the Superabsorbent layer, creates a barrier to external exogenous and polluting bacteria and ensures high breathability. It also ensures optimal fluid management thanks to its high permeability.
The layer in internal polyurethane film that adheres to the polyurethane foam on one side and to the silicone on the other, creates an intermediate layer that prevents the delamination of the foam in the presence of humid environment.
The outer layer of silicone adhesive in contact with injury and skin, is perforated (with patented Coloplast technology) along the entire surface of both foam and edge.
The silicone adhesive layer is delicate and does not cause injury during changes and application of the dressing.
The perforation at the polyurethane foam allows the passage of the exudate towards the absorbent layer of the dressing, and also guarantees a safe adherence of the dressing.
The perforation on the edges ensures adequate breathability and evaporation of moisture from the skin.
Directions
Acute and chronic skin lesions from medium to highly exudatory.
Biatain Silicone helps prevent postoperative flittene.
Average dwell time (medium to highly exuding lesions and ulcers): 3-4 days.
Maximum time on site: 7 days.
Contraindications and incompatibilities
In case of allergic reactions, please contact Coloplast for information on components.
Biatain medications and secondary medicines must be removed before radioactive treatment (X-rays, ultrasound treatment, diathermia and microwave).
Do not use Biatain dressings with oxidizing solutions such as hypochlorite and hydrogen peroxide.
Composition
Polyurethane film, polyurethane foam, cellulose fibre (CMC), sodium polyacrylate, polyethylene, adhesive (PSA), perforated Silicone adhesive layer.
Sterilization
Biatain Silicone is sterilized with ethylene oxide.
The lot number and expiry date appear on each package.
Validity
3 years from the date of production, unless otherwise indicated in the package.
Codes
Packaging
Indications on Primary Packaging (User Unit)
Disposable product, CE mark, manufacturer's indication, batch production code, expiry date, manufacturing indication without natural rubber latex, microbiological status (extermination steering), handling information, usage instructions.
Product preservation
Products must be kept at room temperature (25°C).
Disposal
The product does not contain ecotoxic components therefore it does not need special disposal protocols.
Do not disperse in the environment as it is not Biodegradable.
Manufactured without natural rubber latex.
It does not contain phthalates.
Description
The new Biatain Silicone is a multi-layered absorbent dressing consisting of two absorbent layers, two layers in polyurethane film, one external and one internal, and a pressure-sensitive adhesive (PSA) that holds together the two absorbent layers.
The last layer, in contact with the injury and the skin, is made of delicate silicone perforated adhesive.
The first absorbent layer, covered in perforated silicone, consists of Biatain polyurethane foam, multilayered, hydrophilic, with vertical alveolar structure.
Thanks to the special 3D vertical alveolar technology it absorbs and avoids the release of the exudate even under compression, thus creating the ideal humid environment for the healing process of the injury, and avoiding the maceration of the perilesional skin.
Polyurethane foam is positioned without steps at the same level of injury avoiding any pressure marks on the perilesional skin.
In contact with the exudate the foam conforms optimally to the lesion bed reducing the dead spaces where bacteria can nest.
The second absorbent layer, superior to the first, in contact with the external polyurethane film, is a superabsorbent hydrocapillary buffer consisting of polyethylene, cellulose fibre (CMC) and SAP (Super Absorbent particles in sodium polyacrylate polymers).
The instantaneous absorption of the excess exudate that passes through the first layer of polyurethane foam, gives the effect of hydrocapillary to the super absorbent tampon: fluids are absorbed vertically and distributed both vertically and horizontally.
In fact, cellulose and SAP polymers in contact with the exudate change phase, freezing.
The gel that is formed allows to maintain the optimal humid environment for the healing of injuries and to ensure a high level of retention even under compression.
The two absorbent layers are held together by the PSA, Sensitive Pressure Sticker, which prevents the delamination of absorbent layers when they come into contact with moisture following the absorption of the exudate.
The external polyurethane film layer, in direct contact with the Superabsorbent layer, creates a barrier to external exogenous and polluting bacteria and ensures high breathability. It also ensures optimal fluid management thanks to its high permeability.
The layer in internal polyurethane film that adheres to the polyurethane foam on one side and to the silicone on the other, creates an intermediate layer that prevents the delamination of the foam in the presence of humid environment.
The outer layer of silicone adhesive in contact with injury and skin, is perforated (with patented Coloplast technology) along the entire surface of both foam and edge.
The silicone adhesive layer is delicate and does not cause injury during changes and application of the dressing.
The perforation at the polyurethane foam allows the passage of the exudate towards the absorbent layer of the dressing, and also guarantees a safe adherence of the dressing.
The perforation on the edges ensures adequate breathability and evaporation of moisture from the skin.
Directions
Acute and chronic skin lesions from medium to highly exudatory.
Biatain Silicone helps prevent postoperative flittene.
Average dwell time (medium to highly exuding lesions and ulcers): 3-4 days.
Maximum time on site: 7 days.
Contraindications and incompatibilities
In case of allergic reactions, please contact Coloplast for information on components.
Biatain medications and secondary medicines must be removed before radioactive treatment (X-rays, ultrasound treatment, diathermia and microwave).
Do not use Biatain dressings with oxidizing solutions such as hypochlorite and hydrogen peroxide.
Composition
Polyurethane film, polyurethane foam, cellulose fibre (CMC), sodium polyacrylate, polyethylene, adhesive (PSA), perforated Silicone adhesive layer.
| Product | Absorption g/m2, 1 hour | Absorption g/m2, 24 hours | Absorption under compression g/m2, 24 hours | Permeability (MVTR) g/m2, 24 hours | Fluid management (FHC) g/m2, 24 hours |
| Super-absorbent polyurethane foam dressing with silicone adhesive layer | 13860 | 9100 | 10460 | 7400 | 16500 |
Sterilization
Biatain Silicone is sterilized with ethylene oxide.
The lot number and expiry date appear on each package.
Validity
3 years from the date of production, unless otherwise indicated in the package.
Codes
| Type | Commercial code | Size (cm) | Code CND | ISO code | GMDN code |
| Polyurethane foam medicine with silicone adhesive | 33434 | 7.5x7.5 | MANUFACTURE FROM MATERIALS OF ANY HEADING | 09.21.12.003 | 44970 |
| Polyurethane foam medicine with silicone adhesive | 33435 | 10x10 | MANUFACTURE FROM MATERIALS OF ANY HEADING | 09.21.12.003 | 44970 |
| Polyurethane foam medicine with silicone adhesive | 33436 | 12.5 | MANUFACTURE FROM MATERIALS OF ANY HEADING | 09.21.12.003 | 44970 |
| Polyurethane foam medicine with silicone adhesive | 33437 | 15x15 | MANUFACTURE FROM MATERIALS OF ANY HEADING | 09.21.12.003 | 44970 |
| Polyurethane foam medicine with silicone adhesive | 33438 | 17,5x17,5 | MANUFACTURE FROM MATERIALS OF ANY HEADING | 09.21.12.006 | 44970 |
| Polyurethane foam medicine with silicone adhesive | 33400 | 10x20 | MANUFACTURE FROM MATERIALS OF ANY HEADING | 09.21.12.003 | 44970 |
| Polyurethane foam medicine with silicone adhesive | 33401 | 10x30 | MANUFACTURE FROM MATERIALS OF ANY HEADING | 09.21.12.006 | 44970 |
| Polyurethane foam medicine with silicone adhesive | 33404 | 15x19 Sacred | MANUFACTURE FROM MATERIALS OF ANY HEADING | 09.21.12.012 | 44970 |
| Polyurethane foam medicine with silicone adhesive | 33405 | 25x25 | MANUFACTURE FROM MATERIALS OF ANY HEADING | 09.21.12.012 | 44970 |
| Polyurethane foam medicine with silicone adhesive | 33406 | 18x18 Tallion | MANUFACTURE FROM MATERIALS OF ANY HEADING | 09.21.12.012 | 44970 |
| Polyurethane foam medicine with silicone adhesive | 33408 | 14x19,5 Multisite | MANUFACTURE FROM MATERIALS OF ANY HEADING | 09.21.12.012 | 44970 |
Packaging
| Units of use | 1 single package dressing |
| 33434 | 10 units of use 135 x 147 mm |
| 33435 | 10 units of use 165 x 177 mm |
| 33436 | 10 units of use 166 x 177 mm |
| 33437 | 5 units of use 220 x 227 mm |
| 33438 | 5 units of use 226 x 227 mm |
| 33400 | 5 units of use 150 x 250 mm |
| 33401 | 5 units of use 350 x 150 mm |
| 33404 | 5 units of use 200 x 250 mm |
| 33405 | 5 units of use 300 x 300 mm |
| 33406 | 5 units of use 230 x 250 mm |
| 33408 | 5 units of use 190 x 250 mm |
Indications on Primary Packaging (User Unit)
Disposable product, CE mark, manufacturer's indication, batch production code, expiry date, manufacturing indication without natural rubber latex, microbiological status (extermination steering), handling information, usage instructions.
Product preservation
Products must be kept at room temperature (25°C).
Disposal
The product does not contain ecotoxic components therefore it does not need special disposal protocols.
Do not disperse in the environment as it is not Biodegradable.
- Deductible product
- Yes
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