Ci dedichiamo all’innovazione dei dispositivi di sutura.
Dallo sviluppo dei primi dispositivi di sutura chirurgica all’attuale design avanzato delle suture Tri-Staple™, Medtronic continua a dedicarsi ai tipi di innovazione delle suture a cui si affidano i nostri clienti.
In Medtronic sfruttiamo oltre 50 anni di esperienza per fornire ai nostri clienti soluzioni costanti e di alta qualità per interventi chirurgici a cielo aperto e mininvasivi.
Il sistema di sutura Signia™ funziona con tutte le ricariche per suturatrici Medtronic presenti e future e, se usato insieme alle ricariche Tri-Staple™ 2.0, fornisce feedback in tempo reale per facilitare il processo decisionale chirurgico.6
La tecnologia Tri-Staple™ è un’innovazione per la sutura di Medtronic che negli ultimi anni ha trasformato la sutura endoscopica ed è ora destinata a fare altrettanto nelle procedure a cielo aperto.
Le ricariche Tri-Staple™ presentano alcune differenze fondamentali rispetto alle tecnologie precedenti, offrendo una serie di vantaggi clinici per voi e per i vostri pazienti.7,8,9
† Preclinical results may not correlate with clinical performance in humans.
‡ Based on the addition of a third row of staples in the EEA™ circular stapler with Tri-Staple™ technology, as compared to predicate two row device designs.
§ Compared to two-row staplers.
1. Based on internal test report #2128-194, Comparison of EEA™ circular stapler with Tri-Staple™ technology to EEA™ circular stapler with DST Series™ technology in colocolonic and gastrojejunal anastomoses. Aug. 20, 2015.
2. Based on internal test report #RE0036707, Pilot: comparison of EEA™ circular stapler with Tri-Staple™ technology to EEA™ circular stapler with DST Series™ technology in an esophago-gastrostomy using a canine model. Feb. 25, 2015.
3. Based on internal test report #2128-097, Evaluation of early wound healing events in gastrojejunostomies and colonic anastomosis using a three row EEA™ stapler in canines. Aug. 7, 2013.
4. Based on internal test report #PCG-007, Media absorbency under clamped conditions. Aug. 6, 2012.
5. Based on internal test report #2128-002-2, Extrapolation of perfusion studies performed for Endo GIA™ with Tri-Staple™ technology: final analysis of staple line vascularity using MicroCT. April 27, 2015.
6. In base alla dichiarazione 1 delle specifiche dei requisiti software (SRS) e del test 510k.
7. Based on internall sponsored study by ORC International Survey of tissue reinforcement users to determine waste and time loss attributed to separately loaded buttress materials in the OR. Online U.S. national sample of 125 surgeons and 125 OR nurses. November 9, 2011
8. 2183-089 Histology Results-Thoracic GLP (R0058122). 2183-090 Histology Results-Abdominal GLP (R0058123).
9. Based on internal test report #2183-027. Reinforced reload pre-clinical testing, abrasion assessment of staple line reinforcement materials in the thorax of a canine. April 2013; and test report #2183-034. Reinforced reload pre-clinical testing, substantial equivalence chronic study between Neoveil™* and SeamGuard™* in the abdominal cavity of canines. May 2013