CapSure™ provides surgeons the confidence they desire through strong and reliable fixation.
Canada (FR)
CapSure™ provides surgeons the confidence they desire through strong and reliable fixation.
GTIN - null
00801741094996
1
GTIN - null
10801741094993
5
Quantité
5/cs
Dimensions
Système de fixation permanente CapSure™ - 30 attaches
GTIN - null | 00801741094996 | 1 |
GTIN - null | 10801741094993 | 5 |
Quantité | 5/cs |
Dimensions | Système de fixation permanente CapSure™ - 30 attaches |
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informations rapidement et efficacement, veuillez contacter notre équipe chargée des réclamations clients.
Pour faciliter notre enquête, veuillez inclure les informations suivantes dans votre rapport:
1. Bench top data. Results many not correlate to performance in humans.
2 Preclinical data. Results may not correlate to performance in humans
Indications
The CapSure™ Permanent Fixation System is indicated for the approximation of soft tissue and fixation of surgical mesh to tissues during open or laparoscopic surgical procedures, such as hernia repair.
Contraindications
Carefully inspect the area in the vicinity of the tissue being fastened to avoid inadvertent penetration of underlying structures such as bone, nerves, vessels, and viscera. Use of the CapSure™ Permanent Fixation System in the close vicinity of such underlying structures is contraindicated. For reference, the length of the fastener below the fastener head is 3.2 mm, the fastener head is another 1 mm (total 4.2 mm).
Precautions
Adequate counter pressure should be applied on the target area. Avoid placing hand or finger directly over the area where fastener is being deployed to prevent injury. Use caution when applying the CapSure™ fastener over or in proximity to underlying bone, vessels, nerves, or viscera. The intended fixation site should be assessed to ensure that while the tissue is compressed the total distance from the surface of the tissue to any underlying structures is greater than the length of the CapSure™ fastener. Adverse Reactions
Adverse reactions and potential complications associated with fixation devices such as the CapSure™ Permanent Fixation System may include, but are not limited to the following: hemorrhage, pain, edema and erythema at wound site; septicemia/infection; hernia recurrence/wound dehiscence, erosion and allergic response in patients with known sensitivities to PEEK and metals contained in 316L stainless steel, including chromium, nickel, copper, and iron.