Acera Surgical Restrata Wound Matrix Bioabsorbable Wound Dressing 10cm x 12.5cm Meshed
In Stock: 1 Each
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The item listed above is expired and may be used for educational, training, and non-clinical research purposes only. Any product information appearing below, including the product indication statement, pertains to an in-date item only.
Description
Acera Surgical Restrata Wound Matrix
The Restrata™ Wound Matrix is a sterile, single use device intended for use in local management of wounds. The Restrata™ Wound Matrix is a soft, white, conformable, non-friable, absorbable matrix that acts as a protective covering for wound defects, providing a moist environment for the body’s natural healing process to occur.
Product Code: RMESH-4X5
Size: 10cm x 12.5cm Meshed (Coverage: 125 cm2 up to 250 cm2)
Additional Details
- Company Name: Acera Surgical
- Brand Name: Restrata Wound Matrix
- FDA Product Code: FRO
- FDA Product Code Name: Dressing, Wound, Drug
- GMDN Term Code: 64853
- GMDN Term Name: Synthetic Wound Matrix Dressing
- GMDN Term Definition: A sterile bioabsorbable device designed to be applied to hard-to-heal wounds (e.g., diabetic and venous insufficiency ulcers) or burns that involve the dermis, and that provides a matrix of structural synthetic fibres to facilitate the infiltration of native skin elements (e.g., fibroblasts, leukocytes, blood vessels) for skin regeneration; it may in addition be intended to facilitate regeneration of hard tissues such as bone (e.g., in cases of osteomyelitis) and may provide wound exudate absorbency. It does not contain biological materials. This is a single-use device.
Additional information
| Size | 1 |
|---|---|
| Arms | N/A |
| Manufacturer | |
| Unit | box of 1 |
- FDA Product Code: FRO
- FDA Product Code Name: Dressing, Wound, Drug
- GMDN Term Code: 64853
- GMDN Term Name: Synthetic wound matrix dressing
- GMDN Term Description: A sterile bioabsorbable device designed to be applied to hard-to-heal wounds (e.g., diabetic and venous insufficiency ulcers) or burns that involve the dermis, and that provides a matrix of structural synthetic fibres to facilitate the infiltration of native skin elements (e.g., fibroblasts, leukocytes, blood vessels) for skin regeneration; it may in addition be intended to facilitate regeneration of hard tissues such as bone (e.g., in cases of osteomyelitis) and may provide wound exudate absorbency. It does not contain biological materials. This is a single-use device.
