The OptiFix™ Open Absorbable Fixation System was designed for improved ease of use when fixating surgical meshes to the abdominal wall in open ventral hernia procedures by reducing limitations that exist with current laparoscopic straight devices. Combined with Ventrio™ ST, it provides a full system for open ventral hernia repair.
Canada (FR)
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- Présentation
- Spécifications
- Mode d’emploi électronique et ressources
- FAQ
- Produits connexes
- Notifications sur les produits
Optimized Design
For Open Ventral Hernia Repair
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FEATURE AND BENEFIT CARDS NOT AVAILABLE
FEATURE AND BENEFIT CARDS NOT AVAILABLE
GTIN - null
10801741128957
5
GTIN - null
00801741128950
1
Quantité
5 c/s
Dimensions
Système de fixation résorbable ouvert OptiFix™ - 20 attaches résorbables
GTIN
| GTIN - null | 10801741128957 | 5 |
| GTIN - null | 00801741128950 | 1 |
Emballage
| Quantité | 5 c/s |
Spécifications du produit
| Dimensions | Système de fixation résorbable ouvert OptiFix™ - 20 attaches résorbables |
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Élements à prendre en compte
Si vous êtes un patient ou un utilisateur final, vous pouvez nous contacter vous-même, ou vous pouvez demander à votre soignant ou à votre médecin de le faire pour vous. Pour nous aider à traiter vos
informations rapidement et efficacement, veuillez contacter notre équipe chargée des réclamations clients.
Pour faciliter notre enquête, veuillez inclure les informations suivantes dans votre rapport:
- Nom du produit et/ou numéro de catalogue
- Numéro de lot ou numéro de série
- Blessures et/ou préjudices?
- Quel est le problème que vous avez rencontré?
- Est-ce-que l'échantillon réel ou le représentant de l'échantillon est disponible? (Si possible, veuillez envoyer l'échantillon concerné)
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1. Preclinical data on file. Results may not correlate to clinical outcomes.
2. C. R. Bard Inc., bench data on file.
3 Preclinical data on file. Results may not correlate to clinical outcomes.
4 Survey of surgeons attending pre-clinical lab.
Results may not correlate to clinical outcomes. Data on file.
OptiFix™ Open Absorbable Fixation System
Indications
The OptiFix™ Open Absorbable Fixation System is indicated for the fixation of surgical mesh to tissues during open surgical procedures, such as hernia repair.
Contraindications
Contraindications associated with open surgical procedures relative to mesh fixation apply, including but not limited to:
- Fixation of vascular or neural structures
- Fixation of bone and cartilage,
- Situations with insufficient ingrowth of tissue into the mesh over time, which could result in inadequate fixation once the fastener is absorbed.
- Carefully inspect the area in the vicinity of the tissue being fastened to avoid inadvertent penetration of underlying structures such as nerves, vessels, viscera or bone. Use of the OptiFix™ Open Absorbable Fixation System in the close vicinity of such underlying structures is contraindicated. For reference, the length of the fastener below the fastener head is 6.1 mm, the fastener head is another 0.6 mm (total 6.7 mm).
Warnings
The device may not fixate through prosthetics derived from biologic material such as xenografts and allografts. Prosthetic should be evaluated for compatibility prior to use. After use, the OptiFix™ Open Absorbable Fixation System may be a potential biohazard. Handle and dispose of in accordance with any local and federal laws regarding medical waste.
Adverse Reactions
Adverse reactions and potential complications associated with fixation devices such as the OptiFix™ Open Absorbable Fixation System may include, but are not limited to the following: hemorrhage; pain, edema and erythema at wound site; allergic reaction to Poly(D, L)-lactide; infection/septicemia; hernia recurrence/wound dehiscence.
Please consult product labels and inserts for any indications, contraindications, hazards, warnings, precautions and instructions for use.
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