
Product Overview
The Adhesive Foam Wound Dressing is a sterile, single-use polyurethane dressing integrated with a medical-grade polyurethane (PU) film and an adhesive border. Engineered with a porous, absorbent polyurethane foam core, it provides high fluid uptake capacity alongside a breathable, waterproof exterior backing. This dressing is designed for moderate to highly exuding chronic and acute wounds, absorbing wound drainage, maintaining an optimal moist wound healing environment, and protecting the wound bed from external bacterial contamination without requiring secondary fixation tapes.
Technical Specifications
| Item | Specification |
|---|---|
| Product Name | Adhesive Foam Wound Dressing |
| Dressing Type | Adhesive Polyurethane Foam Dressing |
| Base Material / Active Ingredient | Hydrophilic polyurethane foam pad, waterproof PU film backing, medical-grade adhesive |
| Sterility | Sterile (Single use only) |
| Available Sizes | 10 cm × 10 cm, 15 cm × 15 cm (Custom sizes available upon request) |
| Material Structure |
Foam density: 0.090 g/cm³–0.220 g/cm³; Thickness tolerance: ±1 mm; PU film pore size: ≤0.5 μm; Liquid absorption: ≥10.0 g/g; pH: 5.0–9.0 |
| Packaging | Individually packed in sterile peel pouches, 5–10 pcs/box |
| Sterilization Method | Irradiation sterilization |
| Shelf Life | 5 years |
| Storage Condition | Store in a ventilated, dry area at room temperature; avoid direct exposure to sunlight |
| OEM / ODM Support | Supported (Custom sizing, private labeling, packaging configuration) |
Key Features
High fluid uptake capacity – porous polyurethane core absorbs wound fluid (≥10.0 g/g) to help protect periwound skin from breakdown and maceration.
Integrated adhesive border – helps keep the dressing in position without requiring additional fixation tape across most application sites.
Moisture balance maintenance – supports physiological hydration at the wound bed, providing conditions favorable for natural healing.
Waterproof outer film – serves as a functional barrier against moisture and outside contaminants while allowing gas and vapor exchange.
Conformable foam matrix – flexes comfortably over contoured anatomy and provides light mechanical cushioning.
Gentle wound release – non-stick contact interface helps reduce pulling on healing tissue and lessens patient discomfort during dressing changes.
Controlled material purity – low heavy metal content (≤10 ppm) and clean drying profiles help maintain skin tolerance.


Indications & Applications
Designed for moderate to heavily draining partial- and full-thickness wounds across acute and extended care settings:
- Chronic Wounds: Pressure injuries/ulcers, diabetic foot ulcers, and venous or arterial leg ulcers.
- Surgical & Acute Sites: Post-operative incisions, donor sites, and general surgical wounds.
- Minor Traumas & Burns: Skin tears, abrasions, lacerations, and 1st to 2nd-degree thermal burns.
- Secondary Coverage: Can be paired over primary alginate or ribbon fillers in deeper cavitary spaces.
Contraindications: Not intended for third-degree burns, heavily infected sites with uncontrolled drainage, or alongside oxidizing agents such as hydrogen peroxide or hypochlorite solutions.

Sizes & Packaging
| Size | Dressing per Pouch | Pouches per Box |
|---|---|---|
|
10 cm × 10 cm (Pad: approx. 5 cm × 5 cm) |
1 pc | 10 |
|
15 cm × 15 cm (Pad: approx. 10 cm × 10 cm) |
1 pc | 5 |
| Custom Sizes / Die-Cut Shapes | 1 pc | Configurable |
Packaging & OEM Capabilities:
- Individual medical-grade Tyvek/foil or paper-poly peel pouches ensure sterile barrier integrity.
- Inner box and master carton quantities are fully configurable to meet hospital, retail pharmacy, and distributor channel specifications.
- Comprehensive OEM/ODM private labeling services are available, including custom artwork, barcode formats, multilingual IFUs, and specialized border adhesive options (acrylic or silicone).
Quality & Regulatory Information
- ISO 13485
- CE Marking
- FDA Medical Device Listing
- Sterilization Validation: Compliant with radiation sterilization validation protocols
- Biocompatibility Testing: Evaluated for cytotoxicity, skin irritation, and delayed-type sensitization

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