The absorbable tacks provide serious endurance all through the healing procedure with possibly 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 discover du produit avant toute utilisation.
Lower la probabilidad de pinchazos accidentales en el quirófano, ya que no se requieren agujas como guía para el anclaje.
With the AbsorbaTack™ fixation machine, you’ll find out many Added benefits for efficient hernia repair service applying absorbable fixation to protected your mesh.
Este dispositivo no necesita una aguja guía para fijarse, eliminando el riesgo de pinchazos accidentales.
†Bench test success may not essentially be indicative of medical overall performance. ‡Animal info just isn't always indicative of human scientific results.
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Control fulfills self confidence read more with a unique screw style and design that promotes controlled deployment into tissue by permitting the tack to self-tap. Without having for piloting needles to position the tack, there’s no chance for needle sticks.
Minimizes the probability of inadvertent needle sticks during the OR, considering that no sharp piloting needles are needed for deployment
The AbsorbaTack™ device doesn’t need a pointy piloting needle to deploy, eradicating the chance of inadvertent needlesticks while in the OR.
More Information The New AbsorbaTack (ABSTACK30X) fixation device for laparoscopic hernia maintenance continues to deploy tacks if the shaft is flexed over 3 cm. A short Model (ABSTACK20S) is available for open hernia mend.
Minimizes the likelihood of inadvertent needle sticks from the OR, given that no sharp piloting needles are demanded 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
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