Coloplast Restorelle M Mesh, Polypropylene, 15cm x 10cm
In Stock: 17 Eaches
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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
Coloplast Restorelle® Flat Mesh
Restorelle® synthetic mesh incorporates Smartmesh® technology in a customizable implant specifically for sacrocolpopexy procedures.
Restorelle® products incorporate Smartmesh® technology in a full array of customized shapes and flat grafts specifically for pelvic floor repair procedures.
The mesh is intended to be non-palpable to the patient and her partner. It is the first mesh designed by a surgeon, specifically with a woman’s anatomy and tissue healing requirements in mind.
Additional information
| Size | 1 |
|---|---|
| Arms | N/A |
| Manufacturer | |
| Unit | box of 1 |
- FDA Product Code: OTO
- FDA Product Code Name: Mesh, surgical, synthetic, urogynecologic, for apical vaginal and uterine prolapse, transabdominally placed
- GMDN Term Code: 60842
- GMDN Term Name: Pelvic organ prolapse surgical mesh, synthetic polymer
- GMDN Term Description: A sterile woven/knitted or porous material comprised of a non-bioabsorbable synthetic polymer (e.g., polypropylene) intended to be permanently implanted into a female patient for reinforcement and/or bridging of the supporting tissues of the pelvic floor for the surgical treatment of vaginal pelvic organ prolapse (POP), including anterior, posterior, or apical prolapse repair. It is typically available with various material attributes (e.g., density, pore size, weave) and may be pre-configured for specific repair or cut to desired size/shape. Disposable devices associated with implantation (e.g., introducer needles) may be included.
