The absorbable tacks source serious endurance all over the healing procedure with most likely much less adhesions than lasting tack fixation.four,†
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 discover du produit avant toute utilisation.
The AbsorbaTack™ loved ones of merchandise provide mesh fixation Necessities medical professionals can see. You'll be able to believe in you happen to be deploying tacks successfully that has a trustworthy tack deployment in addition to a ratcheted mechanism offering tactile feedback Whilst you hearth.
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Este dispositivo no necesita una aguja guía para fijarse, eliminando el riesgo de pinchazos accidentales.
† Bench exam final results might not automatically be indicative of scientific general performance · ‡ Animal knowledge is not really essentially indicative of human scientific outcomes.
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Management fulfills self-assurance with a singular screw design that encourages controlled deployment into tissue by enabling the tack to self-tap. Without having for piloting needles to put the tack, there’s no possibility for needle sticks.
Cuts down the chance of inadvertent needle sticks during the OR, since no sharp piloting needles are necessary for deployment
The AbsorbaTack™ unit doesn’t require a sharp piloting needle to deploy, getting rid of the potential risk of inadvertent needlesticks from the OR.
More Information The New AbsorbaTack (ABSTACK30X) fixation unit for laparoscopic hernia restore carries on to deploy tacks in the event the shaft is flexed more than 3 cm. A brief version (ABSTACK20S) is readily available for open hernia mend.
Reduces the chance of inadvertent needle sticks during the OR, since no sharp piloting needles are demanded for deployment
Los resultados preliminares del estudio clínico demostraron que hay un fifty four% de reducción del dolor respecto al valor inicial preoperatorio en el seguimiento a un mes1
Minimizes the probability of inadvertent needle sticks from the OR, given that no sharp piloting needles are expected for deployment