501420
Coloplast Restorelle Y Mesh, Polypropylene, 24cm x 4cm
$19.00
box of 1
In Stock: 10 Eaches
Expiration:
Expired
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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.
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Description
Coloplast Restorelle® Y Polypropylene Mesh
Restorelle® incorporates Smartmesh® technology in a full array of customized shapes and flat grafts specifically for sacrocolpopexy procedures.
Surgical Handling and Orientation Ease
- Easily view anatomical landmarks and suture positioning
- Low mesh memory fits through ports and easily rolls and unrolls to assess placement
- Provides procedural efficiency during surgery without having to stitch, lift up mesh
- Large 1.8 mm macropores enable suturing without needles
- Tailored uni-directional design maintains structural integrity from the sacrum to the vagina
- No rough edges or weak seams
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.
