Not known Factual Statements About abstack30
Not known Factual Statements About abstack30
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The absorbable tacks offer actual staying power through the entire therapeutic process with likely less adhesions than everlasting tack fixation.4,†
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 see du produit avant toute utilisation.
The AbsorbaTack™ relatives of products deliver mesh fixation essentials physicians can see. You'll be able to have confidence in you might be deploying tacks efficiently that has a responsible tack deployment and a ratcheted system offering tactile responses When you hearth.
With the AbsorbaTack™ fixation device, you’ll discover many Gains for productive hernia repair employing absorbable fixation to secure your mesh.
Este dispositivo no necesita una aguja guía para fijarse, eliminando el riesgo de pinchazos accidentales.
†Bench examination outcomes may not necessarily be indicative of clinical overall performance. ‡Animal information isn't essentially indicative of human scientific outcomes.
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But the key benefits of mesh fixation with our product transcend that. By structure, the device supports a minimally invasive approach through a five-mm shaft.
Lowers the likelihood of inadvertent needle sticks during the OR, due to the fact no sharp piloting needles are necessary for deployment
The AbsorbaTack™ gadget doesn’t need to have a pointy piloting needle to deploy, eliminating the risk of inadvertent needlesticks inside the OR.
More info The brand new AbsorbaTack (ABSTACK30X) fixation gadget for laparoscopic hernia mend proceeds to deploy tacks in the event the shaft is flexed over 3 cm. A brief version (ABSTACK20S) is available for open up hernia restore.
Decreases the probability of inadvertent needle sticks within the OR, considering the fact that no sharp piloting needles are expected 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
Reduces the likelihood of inadvertent needle sticks while in the OR, considering the fact that no sharp piloting needles are necessary for deployment