Plus the absorbable tack makes sure no international materials continue to be in your body as time passes 5,‡ since there is no steel necessary for mesh fixation. The end result — tacks that vanish and mesh that stays set up.
Le dispositif de fixation Absorbatack™ est un dispositif médical de classe III, fabriqué par Covidien LLC, CE n°0123. Le dispositif Absorbatack™ est utilisé pour le renforcement des tissus mous de la paroi abdominale en présence d’une faiblesse, dans les procédures chirurgicales impliquant les hernies primaires de la paroi abdominale et les hernies incisionnelles. Lire attentivement la observe du produit avant toute utilisation.
Decrease la probabilidad de pinchazos accidentales en el quirófano, ya que no se requieren agujas como guía para el anclaje.
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Expiration dates have mainly to complete with sterilization instead of the integrity on the solution. The producers sterilize the products once they are packaged and it lasts so a few years. The sole products we caution customers about are types which are absorbable or drug coated.
†Bench test results may not essentially be indicative of scientific general performance. ‡Animal data isn't necessarily indicative of human clinical results.
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But some great benefits of mesh fixation with our unit transcend that. By design and style, the product supports a minimally invasive approach via a 5-mm shaft.
Reduces the likelihood of inadvertent needle sticks inside the OR, since no sharp piloting needles are required for deployment
The AbsorbaTack™ unit doesn’t need to have a pointy piloting needle to deploy, getting rid of the chance of inadvertent needlesticks during the OR.
More info The brand new AbsorbaTack (ABSTACK30X) fixation device for laparoscopic hernia mend proceeds to deploy tacks if the shaft is flexed above 3 cm. A short Edition (ABSTACK20S) is accessible for open up hernia restore.
Decreases the chance of inadvertent needle sticks while in the website OR, considering that no sharp piloting needles are necessary for deployment
Los resultados preliminares del estudio clínico demostraron que hay un 54% de reducción del dolor respecto al valor inicial preoperatorio en el seguimiento a un mes1
Minimizes the likelihood of inadvertent needle sticks during the OR, due to the fact no sharp piloting needles are needed for deployment